FDA EIR for HUZHOU ZHANWANG PHARMA (FEI 1000613242) – March 2024 Inspection

FDA EIR for HUZHOU ZHANWANG PHARMA (FEI 1000613242) – March 2024 Inspection

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Original Request: Request to acquire the FDA EIR report for FDA inspection of HUZHOU ZHANWANG PHARMA - FEI: 1000613242. Including any previously FOIA-released documents related to this inspection. Category: Drug Quality Assurance, ending 29 March 2024 Location: West Development Area Rd, Linghu Town, Huzhou, Zhejiang 313018, China (CHN)
Tags: Pharma, EIR, 2024
  • 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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