Food and Drug Administration. FDA or Food and Drug Administration means the United States Food and Drug Administration, or any successor agency.

Food and Drug Administration or "FDA" means the United States Food and Drug Administration.

Food and Drug Administration or "FDA" means the United States government agency responsible for ensuring compliance with the Food, Drug, and Cosmetics Act of 1938.

Examples of Food and Drug Administration in a sentence

Thank you for agreeing to be participate in our study to better educate groups influencing generic drug use, based on their unique educational needs, sponsored by the US Food and Drug Administration (FDA).
U.S. Food and Drug Administration, Center for Food Safety and Applied Nutrition.
A “medically accepted indication” is a use of the drug that is either approved by the Food and Drug Administration or supported by certain reference books.
The service cannot be legally marketed in the United States without the approval of the Food and Drug Administration (“FDA”) and such approval has not been granted.
Purchase cost of full order irrespective of its consumed quantity shall be recovered from contract holder from the outstanding bills or Security Deposit.v. The goods which are not used, but belong to the said substandard batch shall be destroyed by the concerned BMC hospitals/maternity homes/Dispensaries / HBT clinics etc in the presence of/or under intimation to Food and Drug Administration officials.

More Definitions of Food and Drug Administration

Food and Drug Administration means the United States

Food and Drug Administration means the United States government agency responsible for ensuring compliance with the Food, Drug, and Cosmetics Act of 1938.

Food and Drug Administration. ("FDA") shall mean the U.S. Food and Drug Administration.

Food and Drug Administration or “FDA” means the federal governmental body which certifies that a mammography facility meets minimum quality standards for personnel, equipment, and record keeping.

Food and Drug Administration means the food and drug administration in the United States department of health and human services, or any successor entity.

Food and Drug Administration has approved the Product for marketing in the Field as specified in the notice transmitted pursuant to Paragraph 7.01.