FDA Inspection 1012899 — Medion Grifols Diagnostics AG
The FDA completed an inspection of Medion Grifols Diagnostics AG on Mar 2, 2017 in Dudingen. 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
- Mar 2, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Dudingen (Switzerland)