FDA Inspection 1005708 — Bio-Rad Medical Diagnostics GmbH
The FDA completed an inspection of Bio-Rad Medical Diagnostics GmbH on Jan 27, 2017 in Dreieich. 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
- Jan 27, 2017
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Dreieich (Germany)