06/16/2020 12:00 AM EDT
Source: U.S. Food and Drug Administration (FDA). Published: 6/16/2020. This three-page letter, issued on June 16, 2020, is notification of the revocation of the Emergency Use Authorization for the DPP® COVID-19 IgM/IgG System, which received an Emergency Use Authorization from the Food and Drug Administration on April 14, 2020. (PDF)
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