Introduction of U.S. FDA Medical Device Certification

The U.S. FDA is part of the U.S. Department of State's Division of Health Care and Services, Public **** Health Services, is responsible for all U.S. food, drug, cosmetic and radiological device management, it is also the first consumer protection agency in the U.S. The FDA not only collects and handles 80,000 U.S. product samples manufactured in or imported into the U.S. and to implement the test, but also, each year, to send thousands of inspectors to 15,000 plants overseas to confirm that their activities are in compliance with U.S. laws and regulations. The FDA not only collects and processes 80,000 samples of products manufactured or imported into the United States, but also sends thousands of inspectors to 15,000 factories overseas each year to verify that their activities comply with U.S. laws.