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Business · 09/03/2023

FDA Revokes COVID-19 Emergency Use Authorizations for Two Diagnostic Devices

The US Food and Drug Administration (FDA) has revoked two Emergency Use Authorizations (EUAs) for COVID-19 diagnostic devices, issued to Babson Diagnostics, Inc. and Twist Bioscience Corporation, following requests from the authorization holders.

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

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