FDA Inspection 895020 — Pfizer Ireland Pharmaceuticals Unlimited Company
The FDA completed an inspection of Pfizer Ireland Pharmaceuticals Unlimited Company on Jun 17, 2014 in Dublin 22. 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 17, 2014
- Fiscal Year
- 2014
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Dublin 22 (Ireland)