FDA Inspection 989301 — Wyeth Pharmaceutical Division Of Wyeth Holdings LLC
The FDA completed an inspection of Wyeth Pharmaceutical Division Of Wyeth Holdings LLC on Aug 18, 2016 in Sanford, NC. 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
- Aug 18, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Sanford, NC (United States)