Decree No. 330 / 2004 Coll.
Decree on measures to prevent the introduction and spread of harmful organisms of plants and plant products
Valid
Order
Effective from 31.05.2004
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330
DECLARATION
of 4 May 2004
on measures to prevent the introduction and spread of harmful organisms of plants and plant products
The Ministry of Agriculture pursuant to § 88 (1) (b) of Act No. 326 / 2004 Coll., on Phytosanitary Care and on the Amendment of Certain Related Acts (hereinafter "the Act ') provides:
Subject matter and basic terms
(1) This Regulation (1) implements the relevant provisions of the European Communities (hereinafter referred to as the Community) 1a and provides for measures to prevent the introduction and spread of harmful organisms of plants and plant products.
(2) For the purposes of this decree:
(a) a pathogen - a genetically established set of individuals of one type of harmful organism which differs from another genetically established set of individuals of the same species,
(b) indexed - any procedure to demonstrate the presence of phytoplazes, viruses, viroids or similar harmful organisms in susceptible (marker) plants,
(c) played wood - wood free of natural rounded surface,
(d) grain - seeds which are plant products pursuant to § 2 (1) (c) of the Act,
(e) entry point - place where plants, plant products or other objects enter the customs territory of the Community for the first time: in the case of air transport by airport, in the case of sea or river transport by port, in the case of rail transport by rail by railway station, in the case of other transport by rail, the registered office of the customs office in whose territorial jurisdiction the territorial borders of the Community are crossed within its territory;
(f) office of entry - the office in the Member State of the European Union to which the entry point is subject;
(g) office of destination - Office in the Member State of the European Union within the territorial competence of the office of destination,
(h) customs office of entry - office of entry as defined in (e);
(i) office of destination - office of destination 1b);
(j) customs-approved treatment or use - customs-approved design1c),
(k) transit - transport of goods subject to customs supervision from one place to another within the customs territory of the Community (1d).
(3) For the purposes of this decree:
(a) European countries - Albania, Andorra, Belgium, Belarus, Bosnia and Herzegovina, Bulgaria, Czech Republic, Denmark, Estonia, Faeroe Islands, Finland, France, Gibraltar, Croatia, Ireland, Iceland, Italy, Kazakhstan (European Part), Cyprus, Liechtenstein, Lithuania, Latvia, Luxembourg, Hungary, Macedonia, Malta, Moldova, Monaco, Germany, Netherlands, Norway, Poland, Portugal, Austria, Romania, Russia (European Part), Greece, San Marino, Slovakia, Slovenia, United Kingdom of Great Britain and Northern Ireland, Serbia and Montenegro, Spain (including the Canary Islands), Sweden, Switzerland, Turkey (European Part), Ukraine, Vatican,
(b) non-European Mediterranean countries - Algeria, Ceuta, Egypt, Israel, Jordan, Lebanon, Libya, Morocco, Melilla, Syria, Tunisia, Turkey,
(c) North American countries - Greenland, Canada, Saint Pierre and Miquelon, United States of America (USA),
(d) American countries - all countries of North, Central and South America, including the islands;
(e) continental American countries - all countries of North, Central and South America, except the islands;
(f) United States of America - Alabama, Alaska, Arizona, Arkansas, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, South Dakota, South Carolina, California, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Mississippi, Missouri, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New York, New Mexico, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, North Dakota, North Carolina, Tennessee, Texas, Utah, Vermont, New Mexico, Washington, Washington, Washington D. C., Wisconsin, Wyoming, North Virginia.
Survey prior to the establishment of breeding, reproduction or reproduction material
(Paragraph 6 (1) of the Act)
(1) The survey provided for in Article 6 (1) of the Act on the detection of harmful organisms listed in Annex 1 (A) and 2 (A) and, where appropriate, harmful organisms against which measures have been laid down under Article 7 (3) of the Act, the presence of which is an obstacle to recognition under specific legislation2), (3) shall be carried out:
(a) in the case of the crop of fruit and vine propagating material prior to the establishment of plants of Citrus L., Cydonia Mill., Fragaria L., Malus Mill., Prunus L., Pyrus L., Rubus L., Vitis L., intended for the production of breeding material, pre-stage propagating material and basic propagating material; or
(b) for forest reproductive material sources, where they belong to Abies Mill., Castanea Mill., Larix Mill., Picea A. Dietr., Pinus L., Populus L., Prunus L., Pseudotsuga Carr., and Quercus L., before recognising the source of plant reproductive material intended for vegetative reproduction.
(2) The State Plant Health Administration (hereinafter referred to as the "Plant Health Administration") publishes in the Bulletin of the State Plant Health Administration (hereinafter referred to as "Bulletin") a model of the application for the survey referred to in Article 6 (1) of the Act, the manner, date and address of the application point. The application shall include:
(a) the name and surname of the applicant or, where applicable, of the business firm, if it is a natural person, or the name or business name of the applicant, if it is a legal person;
(b) the address of the applicant for service and the registered office, if any,
(c) the name, surname and address of the person authorised by the applicant to deal with the plant health administration for service;
(d) the identification of the parcel on which the crop of propagating material is to be based or the source of reproductive material recognised;
(e) the name of the species of plant whose propagating material is to be grown or the species of plant whose source of reproductive material is to be recognised.
Harmful organisms, plants and plant products which are prohibited from introduction and spread
[Articles 2 (1) (e) and 7 (1) of the Law]
(1) The harmful organisms listed in Annex No 1, Part A, and plants and plant products listed in Annex No 2, Part A, where they are contaminated by harmful organisms listed in Annex No 2, Part A, are prohibited from introduction and spread.
(2) The harmful organisms listed in Annex No 1, Part B are prohibited from introduction into and spread within the protected zones listed in that Part.
(3) Plants and plant products listed in Annex No 2, Part B, are prohibited from introduction into and spread within the protected zones listed in the same part of that Annex if they are contaminated by harmful organisms listed in the same part of that Annex.
(4) The harmful organisms listed in Annexes 1 and 2 are divided into:
(a) organisms not known to occur in any part of the Community are of Community importance and listed in Annex 1, Part A, Section I and Annex 2, Part A, Section I;
(b) organisms known to occur in the Community but not endemic or established throughout the Community are of Community importance and listed in Annex 1, Part A, Section II and Annex 2, Part A, Section II;
(c) other organisms which are relevant for certain protected zones and are listed in Annex 1, Part B and Annex 2, Part B.
(5) Plants, plant products and other objects subject to import and marketing provisions with regard to the definition of wood as provided for in Article 2 (1) (e) of the Act are listed in Annex 9.
Plants, plant products and other objects prohibited from importing and moving
(Paragraph 7 (5) to (7) of the Act)
(1) Plants, plant products and other objects listed in Annex 3, Part A, are prohibited from being imported and moved if they come from countries listed in that Part.
(2) Plants, plant products and other objects listed in Annex 3, Part B, are prohibited from being introduced into the protected zones listed in that Part.
(3) Plants, plant products and other objects listed in Annex No 4, Part A, are prohibited from being imported and moved unless the specific requirements set out in that Part are met.
(4) Plants, plant products and other objects listed in Annex 4, Part B are prohibited from being introduced into and moved within the protected zones listed in the same part of this Annex unless the specific requirements set out in the same part of this Annex are met.
(5) Small quantities of plants, plant products, food or feed for animals originating in third countries not covered by the provisions of Section 7 (5) (c) and (d) of the Act, provided that they do not show any signs of harmful organism infestation and that they are not intended for experimental, scientific or breeding purposes under Section 8 of the Act, shall not exceed:
| 1. ovoce a zelenina kromě hlíz bramboru (Solanum tuberosum L.) | 2 kg |
| 2. řezané květiny a části rostlin tvořící jednu kytici | 1 kytice |
| 3. osivo kromě semen bramboru (Solanum tuberosum L.) | 5 sáčků v originálním balení pro drobný prodej. |
Authorisation for the handling of quarantine material
(K § 8 (1), (2) and (4) of the Act)
(1) The importation, movement and storage of harmful organisms, plants, plant products and other objects referred to in Article 8 (1) of the Act (hereinafter referred to as "quarantine material") may be authorised and handled by the plant health authorities only if the identifiable risk of spreading the harmful organisms referred to in Article 3 (1) to (3) is excluded.
(2) The phytosanitary management shall assess the risk of the spread of the harmful organisms referred to in paragraph 1 when they are imported, moved, stored and handled, or when plants, plant products and other objects are imported and handled on the basis of:
(a) available current scientific knowledge on the relevant harmful organisms, in particular their biology and active dissemination capability;
(b) an evaluation of the professional and technical assumptions of the consignee of the consignment or of the person importing or keeping the relevant harmful organisms in order to prevent them from spreading;
(c) investigations carried out, where appropriate, in the country of origin of the consignment;
(d) the exclusion of the possibility of covert contamination by appropriate methods by the harmful organisms concerned, including laboratory testing.
(3) The application for authorisation to import quarantine material shall contain:
(a) the date of birth, the name and, where applicable, the name and surname of the applicant, or, where applicable, the business name of the natural person, or, where applicable, the name of the applicant and, where applicable, the surname of his / her legal representative, and, where appropriate, the identification number,
(b) the address of the applicant for service,
(c) the name and, where appropriate, the name and surname of the person responsible for the activities with the quarantine material;
(d) the scientific name of the harmful organisms or plants or the names of plant products or other objects;
(e) the type of quarantine material;
(f) the quantity of quarantine material,
(g) the place of origin of the quarantine material with appropriate documentary evidence, including the address of the place of residence and, where appropriate, the place of the exporter;
(h) packaging, mode of transport, estimated date of import;
(i) the duration, nature and objectives of activities with quarantine material, containing at least a summary of the work process and a specification of experiments for research or breeding purposes;
(j) the address and description of the place where the quarantine material will be maintained and officially tested, if necessary, before being transmitted to the consignee;
(k) the place of first storage or first cultivation after the official release of the quarantine material from the arrangements referred to in paragraph 7, where appropriate;
(l) the proposed procedure for the destruction or treatment of quarantine material after the completion of operations with that material;
(m) the proposed entry point.
(4) The application for authorisation for the possession, reproduction and other handling of quarantine material contains:
(a) the date of birth, the name and, where applicable, the name and surname of the applicant, or, where applicable, the business name of the natural person, or, where applicable, the name of the applicant and, where applicable, the surname of his / her legal representative, and, where appropriate, the identification number,
(b) the address of the applicant for service,
(c) the name and, where appropriate, the name and surname of the person responsible for the activities with the quarantine material;
(d) the scientific name of the harmful organism;
(e) the address and description of the place where the quarantine material will be kept and, where appropriate, the testing referred to in paragraphs 11 and 12;
(f) the duration, nature and objectives of activities with quarantine material, containing at least a summary of the work process and a specification of experiments for research or breeding purposes;
(g) the proposed procedure for the destruction of the harmful organism and the destruction or treatment of the plants, plant products or other objects concerned after the completion of the authorised quarantine material activities, where appropriate;
(h) a draft of the applicant's specific procedures and measures to comply with the principles set out in Annex 5.
(5) In places and facilities where the quarantine material is stored, reproduced or otherwise handled, it shall be ensured that all harmful organisms are under control and in order to avoid their leakage. For each activity referred to in the application referred to in paragraphs 3 and 4, the plant health authorities shall determine the risk of leakage of the harmful organisms referred to in paragraph 1, taking into account the type of quarantine material and the expected activity, the biology of the harmful organisms, their means of spread, their interaction with the environment and other relevant factors associated with the risks posed by the quarantine material.
(6) Plant health management before its decision is taken
(a) verify that the activities for which quarantine material is to be imported or for which harmful organisms are to be kept comply with the concept of work for research, breeding and, where appropriate, diagnostic purposes;
(b) verify that the conditions under which activities with quarantine material are to be carried out comply with the principles set out in Annex 5;
(c) limit the authorised quantity of quarantine material to the quantity necessary for operations with such material and not exceeding the capacity of the appropriate workplace established for these purposes;
(d) examine the professional and technical qualifications of the person responsible for carrying out activities with quarantine material.
(7) The decision to authorise or authorise the import of quarantine material, the storage, reproduction and other handling thereof, in accordance with the principles set out in Annex 5 and the procedures referred to in paragraph 11, shall lay down the specific conditions which must be met and complied with (hereinafter referred to as the quarantine regime), including the means of reporting the possible release of harmful organisms referred to in paragraph 1 from, or their penetration into, the sites or facilities. The person responsible for carrying out the activities of the quarantine material shall request the release of that material from the quarantine regime in advance in order to rule out the hidden assault procedures referred to in paragraph 11 and to carry out the inspection referred to in paragraph 13. The plant health administration may also lay down specific requirements to be met by the imported consignment as well as conditions for the release of quarantine material from the quarantine regime. The authorisation for the possession, reproduction and other handling of quarantine material shall be issued for a period of five years from the date of its issue.
(8) The authorisation form for the import or transfer of quarantine material issued by the plant health authorities pursuant to Article 8 (2) of the Act is set out in Annex 6. When imported or moved, the quarantine material shall be transported to the place of storage without delay.
(9) Where the quarantine material is also a plant, plant product or other object which must be accompanied by a phytosanitary certificate in accordance with Article 23 of the Act on importation, it shall be indicated in the section "Additional declaration" of the phytosanitary certificate: "This material is imported under Directive 95 / 44 / EC" and the specific requirements laid down by the decision of the phytosanitary authority on import authorisation and referred to in the authorisation referred to in paragraph 8 shall be complied with.
(10) Where a plant passport is issued in accordance with Article 12 (1) and (2) for the movement of quarantine material into the territory of the Member States of the European Union, it shall state "This material is moved under Directive 95 / 44 / EC '.
(11) The procedures for the exclusion of a hidden attack on quarantine material intended for experimental, scientific and breeding purposes by harmful organisms are set out in Annex 7.
(12) The condition for the release of quarantine material from the quarantine regime shall be that the conditions laid down in paragraph 7 of this Regulation are complied with and the exclusion of hidden contamination of quarantine material by the procedures referred to in paragraph 11, carried out by trained personnel of the plant health administration or by authorised persons under § 71 (1) (b) or § 72 (5) (i) of the Act, where the quarantine material is found free from harmful organisms, except those known to occur in the Czech Republic and not listed in Annexes 1, 2 and 7 to this Decree or not harmful organisms under § 7 (3) of the Act.
(13) The plant health service shall check at appropriate times, but always before releasing quarantine material from the quarantine regime, compliance with the conditions laid down in paragraph 7, in particular:
(a) procedures for the exclusion of concealed attacks have been carried out by trained staff of the plant health administration or by persons authorised under § 71 (1) (b) or § 72 (5) (i) of the Act;
(b) the quarantine material intended for release from the quarantine regime which has not been found free of harmful organisms as referred to in paragraph 12 and all other plants, plant products and other objects which have been in contact with it or which may have been contaminated have been destroyed or subjected to other measures to destroy the harmful organisms concerned, in the manner laid down by the plant health authority;
(c) other quarantine material and other material found to be infected with harmful organisms during the course of activity and all other plants, plant products and other objects with which it has been in contact or with which it may have been infected have been destroyed or otherwise treated as provided for by the plant health authority;
(d) the places and facilities which were used for the holding, reproduction or other handling of the quarantine material have been sterilised or otherwise treated, where appropriate, in the manner laid down by the plant health authority.
Harmful organisms subject to reporting requirements
(K § 9 of the Act)
Harmful organisms subject to reporting obligations under Article 9 of the Act are listed in Annexes 1 (A) and 2 (A).
Monitoring and exploration of invasive harmful organisms
(Paragraph 10 (1) of the Act)
Invasive harmful organisms subject to monitoring and exploration pursuant to Section 10 (1) of the Act are listed in Annex 8.
Registration or absence of harmful organisms
(Paragraph 10 (4) of the Law)
(1) The registration of the presence or absence of harmful organisms listed in Annexes 1, 2 and 8 and the registration of the first occurrence of harmful organisms which have not yet been known to occur in the Czech Republic contains the following information:
(a) the scope and results of the monitoring and survey carried out under Article 10 (1) of the Act;
(b) the scientific name and, where appropriate, the pathogen of the harmful organism and its taxonomic classification;
(c) the identification of the parcels and objects on or in which the presence of the harmful organism has been detected;
(d) identification of the owner of the land or objects referred to in (c), or of a person who uses them for other legal reasons - name and surname, date of birth or, where applicable, business name, if any, of the natural person or name of the firm, if any, of the legal person, and, where appropriate, the identification number, if any, and the address for service;
(e) the scientific name of the species and, where appropriate, the variety of the host plant,
(f) the date and manner of detection of the harmful organism and the identification of the person who found it;
(g) the identification of the person who has designated the harmful organism and, where appropriate, the person who has verified the accuracy of the determination and the date of the determination and, where appropriate, its verification;
(h) data on the presence of the harmful organism;
(i) the method and outcome of the official verification of the accuracy of the information on the presence of harmful organisms referred to in paragraph 1 provided by natural and legal persons to the plant health authorities.
(2) The register shall also include official documents on the regulations and the implementation of emergency plant health measures ordered under Article 76 (2) of the Act and on information on the presence of harmful organisms referred to in paragraph 1 provided by natural and legal persons to the plant health authorities.
Notification of the presence of harmful organisms to the European Commission
(K § 10 (5) of the Act)
The Plant Health Administration shall notify the European Commission ("the Commission ') and the other Member States of the European Union of the occurrence of:
(a) harmful organisms listed in Annex 1, Part A, Section I and Annex 2, Part A, Section I, throughout the territory of the Czech Republic;
(b) harmful organisms listed in Annex 1, Part A, Section II or Part B and Annex 2, Part A Section II or Part B in that part of the territory of the Czech Republic where their occurrence has not yet been known.
Registration of legal and natural persons
(Paragraph 12 (2) and (7) of the Law)
(1) Plants, plant products and other objects to which the obligation to register natural and legal persons ("plants at risk") applies pursuant to:
(a) Paragraph 12 (1) (a) of the Act is set out in Annex 9, Part A;
(b) Paragraph 12 (1) (b) of the Act is set out in Annex 9, Part B;
(c) Paragraph 12 (1) (c) of the Act is set out in Annex 10.
(2) The plant health service publishes in the Bulletin and on its website a model application for registration in accordance with Section 12 (7) of the Act, the method of application and the address of the application point. The application shall include:
(a) the date of birth, the name and, where applicable, the name and surname of the applicant, or, where applicable, the business name of the natural person, or the name or business name of the applicant, if any, of the legal person, and the identification number, if any, if any;
(b) the address of the applicant for service and the registered office, if any,
(c) the name and, where appropriate, the name, surname and address of the person or persons empowered by the applicant to negotiate with the plant health authority for service;
(d) the range of activities for the risk plants listed in Annex 9 which the applicant intends to place on the market, where appropriate
(e) whether the applicant also requests authorisation to issue plant passports pursuant to Article 17 (1), (2) or (4) of the Act; in this case, the applicant shall attach the design of the plant passport in accordance with Article 17 (2) of the Act.
(3) The register provided for in Article 12 (7) of the Act contains:
(a) the date of birth, the name and surname of the registered person or, where applicable, the business name of the natural person or, where applicable, the name or business name of the registered person, if applicable, the legal person, and the identification number, if assigned,
(b) the address to be served and the registered person's registered office, if any,
(c) the registration number assigned to the registered person by the plant health administration;
(d) whether or not a registered person intends to import or place on the market and has been authorised to issue plant passports under Article 17 of the Act;
(e) details of the termination, interruption, renewal or modification of the activity for which registered persons are registered.
(4) The register shall be kept by the plant health service in electronic form.
Obligations of registered persons
[Articles 13 (1) (a) and 13 (2) of the Law]
(1) Registered persons shall keep a continuous record of the risk plants listed in Annex 9 to their registration. The record shall include:
(a) records of species, varieties and quantities of plants at risk, including categories and generations of propagating or reproduction material, 4)
(b) records and documents of origin, purpose of production, cultivation, handling, import and storage of plants at risk and their transfer or transfer to other persons;
(c) records of places under specific legislation, (5) where risk plants are grown, produced, stored or otherwise handled;
(d) records and documents relating to the care and evaluation of the health status of plants at risk, including records of inspections carried out by a registered person under Article 13 (1) (c) of the Act;
(e) records of plant health checks carried out by the plant health administration and records of plant passports issued by the plant health administration or registered person with the data referred to in Article 15 (2) (d) to (g), including the date of their issue.
(2) The records and documents referred to in paragraph 1 shall be kept by registered persons for at least one year from the date on which the last transfer or transfer of rights to risk plants took place.
(3) The plant health service may, in accordance with Article 13 (2) of the Act, order the registered person to carry out the necessary actions to meet the specific requirements of Annex 4, Part A, Section II and Part B.
Movement of plants, plant products and other objects
(Paragraph 14 (1) and (2) of the Law)
(1) Plants, plant products and other objects which may not be moved within the territory of the Member States of the European Union, provided that the plant passport or replacement plant passport is not attached to them, to their packaging or to the means of transport which transport them, are listed in Annex 9, Part A, point I.
(2) Plants, plant products and other objects which may not be moved to the relevant protected zone listed in Annex 4, Part B and within that zone, provided that the plant passport for the protected zone is not attached to them, to their packaging or to the means of transport which transport them, are listed in Annex 9, Part A, point II.
(3) In accordance with Article 14 (2) of the Act, consignments of seed accompanied by proof of compliance with the specific requirements laid down in Annex 4, Part A, Section II may be moved within the territory of the Member States of the European Union without plant passports.
Continuous phytosanitary inspection
(Paragraph 15 (1) of the Law)
(1) Plants, plant products and other objects which must be subjected to systematic plant health checks before being placed on the market are listed in Annex 9, Part A, point I. This check shall identify the infestation of harmful organisms listed in Annexes 1 (A) and 2 (A) and, where appropriate, the infestation of harmful organisms against which the introduction and spread of which have been provided for in Article 7 (3) of the Act, and verify compliance with the specific requirements set out in Annex 4 (A) (II).
(2) Plants, plant products and other objects which must be subjected to systematic plant health control before being moved to the protected zone are listed in Annex 9, Part A, point II. This check shall identify the infestation of the harmful organisms referred to in paragraph 1 and in Annexes 1 (B) and 2 (B) and verify compliance with the specific requirements referred to in paragraph 1 and Annex 4 (B).
(3) The specific requirements for the verification of the performance of which are carried out in accordance with Article 15 (1) of the Act are set out in Annex 4, Part A, Section II and Part B.
(4) Plants, plant products and other objects the plant health control of which may be carried out on the premises and premises of persons registered under § 12 (1) (c) of the Act are listed in Annex 10.
Authorisation to issue plant passports
(Paragraph 17 (1) and (2) of the Act)
(1) The plant health administration shall issue a plant passport to a person registered in accordance with § 12 (1) (a) and (b) of the Act on the basis of its request to the place of work of the plant health authority responsible for:
(a) the place where the plant health inspection is carried out on importation, if it concerns imported plants, plant products or other objects; or
(b) the place where the land or objects on which the plants, plant products or other objects on which the passports are to be displayed are located;
and in good time before their expected relocation.
(2) The plant health administration may grant for an indefinite period written authorisation for the issue of plant passports and plant passports for a protected zone pursuant to Article 17 (2) of the Act or, where appropriate, replacement passports pursuant to Article 17 (4) of the Act, provided that the authorisation is requested by the registrant in the registration application referred to in Article 10 (2) or by a registered person on the basis of an application the model of which is set out in Annex No 11.
Forms and formalities of plant passports
(Articles 16 (2) and 18 (2) of the Law)
(1) The plant passport shall consist of an official label and, where appropriate, an accompanying document containing the particulars referred to in paragraphs 2 and 3 respectively. The label shall be unused and shall be made of material which prevents its deterioration or damage and shall be affixed to the relevant plants, plant products and other objects, their packaging or means of transport so that it cannot be reused. Any document normally used in the course of trade shall be regarded as an accompanying document. An accompanying document shall not be required if all the particulars referred to in paragraph 2 are indicated on the label.
(2) The plant passport comprising only a label contains the following particulars:
(a) the designation "ES Plant Health Passport,"
(b) identification of the country code;
(c) the designation of the responsible official plant protection organisation of the Member State or its distinguishing mark for plant passports issued in the Czech Republic the designation "State Plant Health Administration" or "SRS,"
(d) the registration number assigned to the registered person responsible for the official plant protection organisation of the Member State for plant passports issued in the Czech Republic by the plant health administration;
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Regulation Information
| Citation | Decree No. 330 / 2004 Coll., on measures to prevent the introduction and spread of harmful organisms of plants and plant products |
|---|---|
| Regulation Type | Order |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 31.05.2004 |
|---|---|
| Effective from | 31.05.2004 |
| Effective until | - |
| Status | Valid |
The regulation text is for informational purposes only.
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