FDA Inspection 816229 — Octapharma Pharmazeutika Produktionsgesellschaft M.B.H.
The FDA completed an inspection of Octapharma Pharmazeutika Produktionsgesellschaft M.B.H. on Dec 18, 2012 in Vienna. 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
- Dec 18, 2012
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Vienna (Austria)