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The FDA regulates thousands of products imported into the U.S. daily, overseeing food supply, drugs, medical devices, biologics, cosmetics, tobacco, and radiation-emitting products. Understanding the FDA's import process is crucial for importers to ensure compliance with regulations, as failure to do so can result in goods being denied entry. It is essential for importers to collaborate with suppliers to meet all FDA requirements, as this not only ensures safety for consumers but is also mandated by law. The FDA's import process consists of five main phases: 1. Preparing to import, 2. Entry submission, 3. Entry review, 4. Examination.