FDA Inspection 791614 — Ziehm Imaging Gmbh
The FDA completed an inspection of Ziehm Imaging Gmbh on Jun 28, 2012 in Nuremberg. 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: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 28, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Nuremberg (Germany)