FDA Inspection 929269 — Bytec Medizintechnik GmbH
The FDA completed an inspection of Bytec Medizintechnik GmbH on Apr 29, 2015 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
- Apr 29, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Eschweiler (Germany)