The U.S. Food and Drug Administration, or FDA, is one of the executive agencies of the U.S. government within the Department of Health and Human Services (DHHS) and the Department of Public **** Health (PHS).
As a scientific regulatory agency, the FDA's responsibility is to ensure the safety of food, cosmetics, drugs, biologicals, medical devices, and radiological products manufactured in or imported into the United States. It was one of the first federal agencies whose primary function was to protect consumers.
Certification significance
The U.S. FDA is part of the U.S. Department of State's Department of Health Care and Services, Public **** Health Services, is responsible for the U.S. all related to the regulation of food, drugs, cosmetics and radioactive devices, it is also the first U.S. consumer protection agency.
The FDA not only collects and processes 80,000 samples of products manufactured or imported into the U.S. and examines them, but also sends thousands of inspectors to 15,000 factories overseas each year to verify that their activities comply with U.S. law.
Since 1990, the FDA has worked closely with international organizations such as ISO to promote a series of innovations. Only declared products after human use of the product after 143 key test points for monitoring, 2-3 million people for 3-7 years of continuous monitoring, completely through the qualified products, will be issued FDA certification.
Reference: Baidu Encyclopedia-FDA