FDA Inspection 1099585 — Curetis GmbH
The FDA completed an inspection of Curetis GmbH on Feb 14, 2019 in Bodelshausen. 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
- Feb 14, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bodelshausen (Germany)