Zdrowie i gospodarka · 15/07/2022
FDA Revokes Emergency Use Authorization for COVID-19 Diagnostic Device
The US Food and Drug Administration (FDA) has revoked the Emergency Use Authorization (EUA) for the ScienCell SARS-CoV-2 Coronavirus Real-time RT-PCR (RT-qPCR) Detection Kit, issued to ScienCell Research Laboratories, due to reasons outlined in the revocation document.
Source: Federal Register — Food and Drug AdministrationOpen original release →