FDA Inspection 1062912 — Joimax GmbH
The FDA completed an inspection of Joimax GmbH on Jul 4, 2018 in Karlsruhe. 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
- Jul 4, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Karlsruhe (Germany)