FDA Inspection 1061483 — Celfa S.C.

Celfa S.C. — FEI 3011480204

The FDA completed an inspection of Celfa S.C. on Jul 20, 2018 in Verona. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 20, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Verona (Italy)

Citations

IDCFRDescription
312321 CFR 820.80(c)Lack of or inadequate In-process acceptance procedures