FDA Inspection 1238306 — Citieffe Srl
The FDA completed an inspection of Citieffe Srl on Feb 15, 2024 in Calderara Di Reno. 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 15, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Calderara Di Reno (Italy)