FDA, short for food and drug administration, is one of the executive agencies established by the U.S. government in the Department of health and human services (DHHS) and the Department of public health (PHS). As a scientific regulatory agency, FDA is responsible for ensuring the safety of food, cosmetics, drugs, biological agents, medical equipment and radiation products produced or imported in the United States. It is one of the earliest federal agencies whose main function is to protect consumers. This institution is closely related to the life of every American citizen. Internationally, FDA is recognized as one of the largest food and drug regulatory agencies in the world. Many other countries seek and receive help from FDA to promote and monitor the safety of their products.
Traditionally, FDA certification is not certification, but a kind of registration. FDA has no certification.
Food and Drug Administration (FDA) is in charge of the supervision and inspection of food, drugs (including veterinary drugs), medical devices, food additives, cosmetics, animal food and drugs, wine drinks with alcohol content less than 7%, and electronic products; The testing, inspection and certification of the items that the ionic and non-ionic radiation produced in the process of use or consumption of products affects human health and safety. According to the regulations, the above-mentioned products can only be sold on the market after they have been proved safe by FDA inspection.
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