Code of Federal Regulations, Title 21, Food and Drugs, Pt. 800-1299, Revised as of April 1, 2017

The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government.  This print ISBN is the official U.S. Federal Government edition.Title 21 CFR, Parts 800-1299, includes rules, regulations, procedures and administrative procedures associated with the Food and Drug Administration and Department of Health and Human Services (medical devices), medical device quality system regulation, postmarket surveillance, unique device identification, medical device classification procedures, mammography, the Mammography Quality Standards Act, radiological health, tobacco products, the Federal Import Milk Act, the Federal Caustic Poison Act, control of communicable diseases, human tissue intended for transplantation, and more...

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