FDA Inspection 676642 — Angiomed GmbH & Co. Medizintechnik KG
The FDA completed an inspection of Angiomed GmbH & Co. Medizintechnik KG on Mar 25, 2010 in Karlsruhe. 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
- Mar 25, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Karlsruhe (Germany)