FDA Inspection 1043999 — IGEA SPA
The FDA completed an inspection of IGEA SPA on February 20, 2018 in Carpi. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 20, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Carpi (Italy)