FDA Inspection 599820 — PFM Medical Titanium GmbH
The FDA completed an inspection of PFM Medical Titanium GmbH on Jul 9, 2009 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
- Jul 9, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Nuremberg (Germany)