FDA Inspection 1020234 — Wyeth BioPharma Division Of Wyeth Pharmaceuticals LLC
The FDA completed an inspection of Wyeth BioPharma Division Of Wyeth Pharmaceuticals LLC on Apr 28, 2017 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
- Apr 28, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Andover, MA (United States)