Federal Poultry Products Inspection Act definition

Federal Poultry Products Inspection Act means the act so entitled, approved August 28, 1957 (71 Stat. 441), as amended by the Wholesome Poultry Products Act (82 Stat. 791).
Sample 1Sample 2Sample 3
Federal Poultry Products Inspection Act means the act of congress approved August 28, 1957, by the Wholesome Poultry Products Act, 82 Stat. 791; 21 U.S.C. 451.
Sample 1Sample 2Sample 3
Federal Poultry Products Inspection Act means the act of congress approved August 28, 1957, as amended, compiled in 21 U.S.C. § 451 et seq.;
Sample 1Sample 2

Examples of Federal Poultry Products Inspection Act in a sentence

  • Amend rule 21—76.3(189A), introductory paragraph, as follows:21—76.3(189A) Federal Poultry Products Inspection Act regulations adopted.

  • No livestock or poultry carcasses or parts thereof, meat food product or poultry products shall be admitted into any official establishment unless they have been prepared only under inspection pursuant to this act or the Federal Meat Inspection Act or the Federal Poultry Products Inspection Act, or their admission is permitted by rules or regulations prescribed by the secretary under this act.

  • Article applicable to those regulated by federal act.The requirements of this Article shall apply to persons, establishments, poultry, poultry products and other articles regulated under the Federal Poultry Products Inspection Act only to the extent provided for in section 23 of said federal act.

  • The Department is further authorized to recommend to the Secretary of Agriculture such officials or employees of this State as the Commissioner shall designate, for appointment to the advisory committees provided for in section 5 of the Federal Poultry Products Inspection Act; and the Commissioner shall serve as the representative of the Governor for consultation with said Secretary under subsection (c) of section 5 of said act.

  • Provided, however, that the provisions of this section shall not apply to an official establishment which is operating under inspection programs pursuant to the Federal Meat Inspection Act or the Federal Poultry Products Inspection Act.

  • Federal Poultry Products Inspection Act of 1957 and Wholesome Poultry Products Act of 1968 - set federal standards on poultry.

  • Statutory references to the "Federal Poultry Products Inspection Act" shall be deemed to refer to the corresponding provisions of the "North Carolina Poultry Products Inspection Act," Article 49D of Chapter 106 of the North Carolina General Statutes.

  • When different contexts share identifiers there is a potential risk of privacy violation when an entity’s attributes from different contexts are linked together by using that shared identifier (profiling).Once an entity exists in a context, i.e. its identity and identifiers have been created, it can start to act in this context.

  • Amend rule 21—76.3(189A), introductory paragraph, as follows: 21—76.3(189A) Federal Poultry Products Inspection Act regulations adopted.

  • Based on current information, I certify the State Meat and Poultry Inspection Program is “at least equal to” the requirements specified in the Federal Meat Inspection Act (FMIA), the Federal Poultry Products Inspection Act (PPIA), and the Humane Methods of Slaughter Act (HMSA).


More Definitions of Federal Poultry Products Inspection Act

Federal Poultry Products Inspection Act means the federal act compiled in 21 U.S.C. § 451 et seq.;
Sample 1
Federal Poultry Products Inspection Act means the act of congress approved August 28, 1957, as amended by the Wholesome Poultry Products Act.
Sample 1

Related to Federal Poultry Products Inspection Act

  • Medical marijuana concentrate means a specific subset of Medical Marijuana that was produced by extracting cannabinoids from Medical Marijuana. Categories of Medical Marijuana Concentrate include Water-Based Medical Marijuana Concentrate, Food-Based Medical Marijuana Concentrate and Solvent-Based Medical Marijuana Concentrate.

  • Bulk drug substance means any substance that is represented for use, and that, when used in the

  • cGMP means current Good Manufacturing Practice as set forth in the United States Federal Food, Drug, and Cosmetic Act, as amended, and includes all rules and regulations promulgated by the FDA thereunder.

  • Applicable Technical Requirements and Standards means those certain technical requirements and standards applicable to interconnections of generation and/or transmission facilities with the facilities of an Interconnected Transmission Owner or, as the case may be and to the extent applicable, of an Electric Distributor, as published by Transmission Provider in a PJM Manual provided, however, that, with respect to any generation facilities with maximum generating capacity of 2 MW or less (synchronous) or 5 MW or less (inverter-based) for which the Interconnection Customer executes a Construction Service Agreement or Interconnection Service Agreement on or after March 19, 2005, “Applicable Technical Requirements and Standards” shall refer to the “PJM Small Generator Interconnection Applicable Technical Requirements and Standards.” All Applicable Technical Requirements and Standards shall be publicly available through postings on Transmission Provider’s internet website.

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Waste Materials means any Contamination-causing solid, semi-solid, or liquid material discarded, buried, or otherwise present on the Property, and may include sludge, slag, or solid waste materials such as empty containers and demolition debris or materials containing asbestos, lead-based paint, or petroleum or other contaminants.

  • Current Good Manufacturing Practices or “cGMP” means applicable Good Manufacturing Practices as specified in the United States Code of Federal Regulations and/or the EU Good Manufacturing Guidelines, and any successor legislation from time to time, prevailing at the time of the manufacture of the Product.

  • cGMPs means current good manufacturing practices as described in Parts 210 and 211 of Title 21 of the United States’ Code of Federal Regulations, together with the latest FDA guidance documents pertaining to manufacturing and quality control practice, all as updated, amended and revised from time to time;

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • Marijuana products means concentrated marijuana products and marijuana products that are comprised of marijuana and other ingredients and are intended for use or consumption, such as, but not limited to, edible products, ointments, and tinctures.

  • Good Manufacturing Practices or “GMP” shall mean the then current Good Manufacturing Practices as such term is defined from time to time by the FDA or other relevant Governmental Authority having jurisdiction over the development, manufacture or sale of the Product in the Territory pursuant to its regulations, guidelines or otherwise.

  • value of originating materials means the value of such materials as defined in subparagraph (g) applied mutatis mutandis;

  • Marijuana producer means a person who produces marijuana in this state.

  • Marijuana testing facility means an entity licensed to analyze and certify the safety and potency of marijuana.

  • Export and Import Laws means the Arms Export Control Act, the International Traffic in Arms Regulations, the Export Administration Act of 1979, as amended, the Export Administration Regulations, and all other laws and regulations of the United States government regulating the provision of services to non-U.S. parties or the export and import of articles or information from and to the United States of America, and all similar laws and regulations of any foreign government regulating the provision of services to parties not of the foreign country or the export and import of articles and information from and to the foreign country to parties not of the foreign country.

  • MSAA Indicator Technical Specifications document means, as the context requires, either or both of the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Indicator Technical Specifications November 5, 2018 Version 1.3” and the document entitled “Multi-Sector Service Accountability Agreement (MSAA) 2019-20 Target and Corridor-Setting Guidelines” as they may be amended or replaced from time to time;

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • Marijuana wholesaler means a person who purchases marijuana items in this state for resale to a person other than a consumer.

  • Bulk plant means a motor fuel storage and distribution facility that is not a terminal and from

  • Medical marijuana waste or "waste" means unused,

  • WTO GPA country construction material means a construction material that—

  • GMPs means all good manufacturing practices under Title 21 of the United States Code of Federal Regulations, as amended from time to time.

  • Collaborative pharmacy practice means a practice of pharmacy whereby one or

  • Regulated Materials means any hazardous, toxic or dangerous waste, substance or material, the generation, handling, storage, disposal, treatment or emission of which is subject to any Environmental Law.

  • Marijuana-infused products means products that contain marijuana or marijuana extracts and are intended for human use. The term "marijuana-infused products" does not include useable marijuana.

  • Marijuana processor means a person who processes marijuana items in this state.