FDA Inspection 986138 — KBL GmbH
The FDA completed an inspection of KBL GmbH on Sep 2, 2016 in Dernbach. 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
- Sep 2, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Dernbach (Germany)