Business · 10/07/2017
FDA Corrects Notice on Emergency Use of Zika Virus Diagnostic Devices
The Food and Drug Administration is correcting a notice regarding the issuance of Emergency Use Authorizations for in vitro diagnostic devices to detect the Zika virus, which was published with an incorrect docket number, following the 2017 Zika virus outbreak in the Americas.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →