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3.4.8 Federal Initiatives 3.4.8.1 United States Food and Drug Administration (FDA) All sterilization operations of medical devices in the United States must use a validated sterilization process that meets internationally agreed upon voluntary consensus standards recognized by the FDA Center for Devices and Radiological Health (CDRH) (FDA 2023a)

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A pipe with residue, ash, or leftover tobacco can cause issues during screening

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