FDA Inspection 1210373 — KBL GmbH
The FDA completed an inspection of KBL GmbH on June 15, 2023 in Dernbach. 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
- June 15, 2023
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Dernbach (Germany)