FDA Inspection 676642 — Angiomed GmbH & Co. Medizintechnik KG
The FDA completed an inspection of Angiomed GmbH & Co. Medizintechnik KG on March 25, 2010 in Karlsruhe. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- March 25, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Karlsruhe (Germany)
Additional Details
Postmarket Audit Inspections