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The Food and Drug Administration (FDA) is an agency within the U.S. Department of Health and Human Services. It consists of six product centers, one research center, and two offices.
FDA is responsible for
- protecting the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products, medical devices, our nation’s food supply, cosmetics, dietary supplements, and products that give off radiation
FDA's Dockets Management serves as the official repository for the administrative proceedings and rule-making documents for the Food and Drug Administration (FDA), an operating division of the U.S. Department of Health and Human Services.
Food Safety Modernization Act (FSMA)
Includes rules and related programs, guidance documents, training and technical assistance, compliance and implementation tools, along with information about the background of the FSMA and its impact on public health.
Comprehensive list of current guidance documents, with links to texts.
Under the Inspections, Compliance, Enforcement, and Criminal Investigation subsection. Letters available from 2005 to the present.