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FDA 483 for Shire Human Genetic Therapies Inspection Ending Mar 23, 2022 (FEI 3009340644)
FDA 483 for Shire Human Genetic Therapies Inspection Ending Mar 23, 2022 (FEI 3009340644)
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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: Shire Human Genetic Therapies, Inc. Lexington United States End Dates of inspection: 23 Mar 2022 Project Area: Drug Quality Assurance FEI: 3009340644 Investigator(s):Wayne E Seifert, Charles Yuanchia Kuo, PhD, Scott C Lute Classification: VAI
Tags: Pharma, 483, 2022
Tags: Pharma, 483, 2022
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- 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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