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Raffis

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Raffis

Re: None

Saturday, 07/25/2020 7:52:52 PM

Saturday, July 25, 2020 7:52:52 PM

Post# of 97081
FDA revocation of the Emergency Use Authorization (EUA) issued April 28, 2020, for emergency use of certain in vitro diagnostic SARS-CoV-2 ANTIBODY TESTS intended for use as an
antibodies (IgG, or IgG and IgM, or total) to SARS-CoV-2 in human plasma and/or serum.
https://www.fda.gov/media/140351/download
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