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    FDA 483 and EIR for Wyeth BioPharma (Andover) Inspection Ending May 3, 2019 (FEI 1222181)

    FDA 483 and EIR for Wyeth BioPharma (Andover) Inspection Ending May 3, 2019 (FEI 1222181)

    $69.00 USD
    $69.00 USD
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    Original Request: To Whom it May Concern: As permitted by the Freedom of Information Act (FOIA), I am hereby requesting the following document: Form FDA 483 & EIR Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC Andover United States of America End Dates of inspection: 03 May 2019 Project Area: Drug Quality Assurance FEI: 1222181 Investigator(s): Nailing Zhang, Wayne E Seifert, Gunther Boekhoudt, PhD, Amy Devlin, PhD Classification: VAI
    Tags: Pharma, 483, 2019
    • Status: Pending Fast-Track Request
    • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

    NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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