Food and Drug Administration's Food Labeling Regulation: Its Effect on Small Business
United States. Congress. House. Committee on Small Business. Subcommittee on Special Small Business Problems
U.S. Government Printing Office, 1978 - 197 páginas
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action added addition advisory agency amended amount applicable appropriate Association baker baking basis bread Bureau cereal chapter Commissioner Committee common or usual concern concludes considered consumer contain copy cost decision determine documents Drug Administration effect established exemption fats FEDERAL REGISTER final flour Food and Drug guideline hearing Hearing Clerk identity industry inflation impact ingredients interested involved issue JANUARY labeling less LIBRARY OF CONGRESS listed major manufacturers materials matter means meeting ment milk notice nutrients nutritional objections opinion package paragraph percent permit person petition plant practice predominance prepared present procedures proposed protein published pursuant reason received record regulation relating representative request response result revising RULES Russo serving specific standard statement submitted suggested term tion usual name vitamin
Página 124 - ... agency action" includes the whole or a part of an agency rule, order, license, sanction, relief, or the equivalent or denial thereof, or failure to act; and (14) "ex parte communication" means an oral or written communication not on the public record with respect to which reasonable prior notice to all parties is not given, but it shall not include requests for status reports on any matter or proceeding covered by this subchapter.
Página 62 - ... the grounds for the objections. If a hearing is requested, the objections shall state the Issues for the hearing, shall be supported by grounds factually and legally sufficient to Justify the relief sought and •hall Include a detailed description and analysis of the factual Information Intended to be presented In support of the objections In the event that a hearing Is held.
Página 140 - ... because of its toxicity or other potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use...
Página 123 - Section 602 (b) of the act provides for the establishment by regulation of reasonable variations and exemptions for small packages from the required declaration of net quantity of contents. Section 5(b) of the Fair Packaging and Labeling Act provides for the establishment by regulation of exemptions from certain...
Página 133 - A person outside the executive branch may invite an agency representative to attend or participate in a meeting outside agency offices. The agency representative is not obligated to attend or participate, but may do so where it is in the public interest and will promote the objectives of the act.
Página 124 - advisory committee" means any committee, board, commission, council, conference, panel, task force, or other similar group, or any subcommittee or other subgroup thereof...
Página 101 - ... if it consists in whole or in part of any filthy, putrid, or decomposed substance, or if it is otherwise unfit for food; or (4) if it has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health...
Página 64 - Part 1 Regulations for the enforcement of the Federal Food, Drug, and Cosmetic Act and the Fair Packaging and Labeling Act.