This SiteProfile is a report containing information on 22 years of U.S. Food & Drug Administration inspections at the Wyeth BioPharma Division of Wyeth Pharmaceuticals facility located in Andover, MA, United States.
This report is updated through .
Site profiles provide key FDA inspection metrics as well as a comprehensive history of all FDA inspections of the site since the year 2000. Site profiles have proven to be useful as part of the due diligence process as companies evaluate a site for validation, acquisition, partnership, and/or benchmarking purposes. If you will be validating a large number of sites on an on-going basis, you should consider Enforcement Analytics or contact us at [email protected]
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