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Thousands of products regulated by the U.S. Food and Drug Administration (FDA) are imported into the United States daily. The FDA oversees most of the nation's food supply, human and animal drugs, medical devices, biologics, cosmetics, tobacco products, and radiation-emitting products. Importers must understand the FDA's import process and compliance requirements. Collaboration with suppliers to ensure FDA-regulated imports meet standards is essential. The FDA works with all supply chain parties to ensure product safety. Imports must comply with FDA requirements, or they may be denied entry. The FDA import process consists of five phases: 1. preparing to import 2. entry submission 3. entry review 4. examination.
