FDA Inspection 1071168 — Gb Implantat Technologie GMBH
The FDA completed an inspection of Gb Implantat Technologie GMBH on Aug 16, 2018 in Bochum. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 16, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bochum (Germany)