FDA Inspection 788580 — Wyeth BioPharma Division Of Wyeth Pharmaceuticals LLC
The FDA completed an inspection of Wyeth BioPharma Division Of Wyeth Pharmaceuticals LLC on Jun 20, 2012 in Andover, MA. 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
- Jun 20, 2012
- Fiscal Year
- 2012
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Andover, MA (United States)