FDA Inspection 900902 — Siemens AG/Siemens Healthcare GmbH
The FDA completed an inspection of Siemens AG/Siemens Healthcare GmbH on Sep 25, 2014 in Kemnath. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 25, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Kemnath (Germany)