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The U.S. Food and Drug Administration (FDA) regulates thousands of products imported daily into the United States, including food, drugs, medical devices, and cosmetics. Importers must understand the FDA's import process and adhere to its requirements, ensuring compliance is essential for both legal and business reasons. The FDA collaborates with suppliers to ensure safety for American consumers, and non-compliant products may be denied entry. The FDA's import process consists of five key phases: 1) preparing to import, 2) entry submission, 3) entry review, 4) examination, and 5) release. Proper preparation and understanding of these phases are crucial for successful importing.