FDA Inspection 1245848 — Bytec Medizintechnik GmbH
The FDA completed an inspection of Bytec Medizintechnik GmbH on Jul 11, 2024 in Eschweiler. 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 11, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Eschweiler (Germany)