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Business · 10/07/2003

FDA Seeks Public Input on Proposal to Revoke Universal Reagents, Inc.'s Biologics License

The Food and Drug Administration (FDA) is inviting public input on a proposal to revoke Universal Reagents, Inc.'s (URI) U.S. License No. 0887 for manufacturing Source Plasma, citing non-compliance with FDA standards and regulations.

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

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