FDA Inspection 597351 — Biotronik SE & Co. KG
The FDA completed an inspection of Biotronik SE & Co. KG on Jul 2, 2009 in Berlin. 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
- Jul 2, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Berlin (Germany)
Additional details
Postmarket Audit Inspections