FDA Inspection 1031348 — Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
The FDA completed an inspection of Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) on Nov 2, 2017 in Ravensburg. 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
- Nov 2, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Ravensburg (Germany)