Poultry Products Inspection Act definition

Poultry Products Inspection Act means the Federal Poultry and Poultry Products Inspection Act, 21 U.S.C. secs. 451 et seq., Pub. L. 85-172, 71 Stat. 441, and any amendments thereto;
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Poultry Products Inspection Act means the Federal Poultry and Poultry
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Poultry Products Inspection Act means the Federal Poultry and Poultry Products Inspection Act, and any amendments thereto;
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Examples of Poultry Products Inspection Act in a sentence

  • All products delivered shall conform in all respects to applicable standards promulgated under the Federal Food, Drug and Cosmetic Act, the Meat Inspection Act, and the Poultry Products Inspection Act in effect at the time of delivery.

  • Animal products not covered under the Federal Meat Inspection Act or the Poultry Products Inspection Act, such as flesh products from deer, bison, rabbit, quail, wild turkey, geese, ostrich, etc.

  • Game meats (i.e., animal prod- ucts not covered under the Federal Meat Inspection Act or the Poultry Products Inspection Act, such as flesh products from deer, bison, rabbit, quail, wild turkey, or ostrich) may pro- vide required nutrition information on labeling in accordance with the provi- sions of paragraph (a)(2) of this section.

  • The term ‘‘food’’ as used in clause (vi) of this subparagraph includes poultry and poultry prod- ucts (as defined in sections 4(e) and 4(f) of the Poultry Products Inspection Act [21 U.S.C. 453(e) and (f)]), meat and meat food products (as de- fined in section 1(j) of the Federal Meat Inspec- tion Act [21 U.S.C. 601(j)]), and eggs and egg products (as defined in section 4 of the Egg Products Inspection Act [21 U.S.C. 1033]).

  • Any substance used in accordance with a sanction or approval granted prior to the enactment of the Food Additives Amendment of 1958, pursuant to the federal act; the Poultry Products Inspection Act, 21 U.S.C. secs.

  • These updated regulations are necessary to comply with the federal Poultry Products Inspection Act (21 USCA 454, Section 5) which establishes Federal-State Cooperative Poultry Inspection Programs.

  • USDA publication “Guidance for Determining Whether a Poultry Slaughter or Processing Operation is Exempt from Inspection Requirements of the Poultry Products Inspection Act Revision 1, April 2006,” provides detailed information on the requirements for the sale of poultry at markets.

  • All actions taken by Seller in connection with any Recall shall comply fully with the U.S. Federal Food, Drug and Cosmetic Act, the U.S. Federal Meat Inspection Act, the U.S. Poultry Products Inspection Act, and any other applicable laws.

  • Custom exempt establishments are slaughter and processing establishments, which are not subject to the routine inspection requirements of the Federal Meat Inspection Act (FMIA) and the Poultry Products Inspection Act (PPIA), provided the specified operations meet the exemption requirements of Section 23 of the FMIA and Section 15 of the PPIA.

  • Euroclear and Clearstream, Luxembourg participants are financial institutions throughout the world, including underwriters, securities brokers and dealers, banks, trust companies, clearing corporations and certain other organisations.


More Definitions of Poultry Products Inspection Act

Poultry Products Inspection Act means the Act approved
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Poultry Products Inspection Act means the Federal Poultry and Poultry Products Inspection Act; 21 U.S.C. sec. 451 et seq., Public Law 85-172, 71 Stat. 441, and any amendments thereto;
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Related to Poultry Products Inspection Act

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  • Petroleum Products means gasolines and petroleum oil distillates or blend stocks as further described in Item 10.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

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  • 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;

  • Manufacture means the production of products in a factory using labour, materials, components and machinery and includes other related value-adding activities.

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  • Product Know-How means Know-How

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