FDA Inspection 1022011 — Biotronik SE & Co. KG
The FDA completed an inspection of Biotronik SE & Co. KG on Jun 22, 2017 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
- Jun 22, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Berlin (Germany)