FDA Inspection 555272 — Siemens Healthineers AG
The FDA completed an inspection of Siemens Healthineers AG on Dec 3, 2008 in Erlangen. 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
- Dec 3, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Erlangen (Germany)