FDA testing

FDA, short for Food and Drug Administration, is one of the executive agencies established by the US 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, biologics, medical devices, and radiation products produced or imported domestically in the United States. It is one of the earliest federal agencies with consumer protection as its primary function. This institution is closely related to the lives of every American citizen. Internationally, the FDA is recognized as one of the largest food and drug regulatory agencies in the world. Many other countries promote and monitor the safety of their domestic products by seeking and receiving assistance from the FDA.

Traditionally, FDA certification is not certification, but a form of registration or registration. FDA does not issue certificates.

The Food and Drug Administration (FDA) oversees the supervision and inspection of food, drugs (including veterinary drugs), medical devices, food additives, cosmetics, animal food and drugs, wine beverages with an alcohol content of less than 7%, and electronic products; Testing, inspection, and certification of the impact of ionizing and non-ionic radiation generated during the use or consumption of products on human health and safety.

According to regulations, the above-mentioned products must undergo FDA inspection to prove their safety before they can be sold in the market.