Business · 18/04/2022
FDA Revokes Emergency Use Authorizations for COVID-19 Diagnostic Devices
The US Food and Drug Administration (FDA) has revoked five emergency use authorizations for COVID-19 diagnostic devices, including those issued to BillionToOne, Inc. and CENTOGENE US, LLC, due to reasons outlined in the document.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →