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Business · 23/07/2003

FDA Corrects Guidance Document on Reprocessed Medical Devices

The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register on July 8, 2003, due to an error in the docket number of a guidance document related to reprocessed single-use medical devices.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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