FDA Inspection 1238306 — Citieffe Srl
The FDA completed an inspection of Citieffe Srl on February 15, 2024 in Calderara Di Reno. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- February 15, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Calderara Di Reno (Italy)