FDA Inspection 1099573 — Curetis Gmbh
The FDA completed an inspection of Curetis Gmbh on Feb 14, 2019 in Holzgerlingen. 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
- Feb 14, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Holzgerlingen (Germany)