FDA Inspection 804865 — Wyeth Pharmaceutical Division Of Wyeth Holdings LLC
The FDA completed an inspection of Wyeth Pharmaceutical Division Of Wyeth Holdings LLC on Oct 24, 2012 in Pearl River, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 24, 2012
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Pearl River, NY (United States)