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FDA Inspection 804865 — Wyeth Pharmaceutical Division of Wyeth Holdings LLC

Wyeth Pharmaceutical Division of Wyeth Holdings LLC — FEI 2410662

The FDA completed an inspection of Wyeth Pharmaceutical Division of Wyeth Holdings LLC on October 24, 2012 in Pearl River, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 24, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Pearl River, NY (United States)

Facility

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  • 1237528 (VAI Wed Aug 28 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1168201 (VAI Wed Apr 13 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791692 (NAI Wed Jul 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 597355 (NAI Wed Jul 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources