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FDA: Revocation of Two Authorizations of Emergency Use of In Vitro Diagnostic Device for Detection and/or Diagnosis of COVID-19; Availability

Federal Register
May 17, 2024
The Food and Drug Administration has revoked Emergency Use Authorizations issued to Bio-Rad Laboratories Inc., and Fast Track Diagnostics Luxembourg S.á.r.l. (A Siemens Healthineers Company) related to COVID-19 detection and diagnosis tests.
Tagged as
COVID-19 · Legislation and regulations · Pharmacy and prescription drugs