FDA Inspection 597361 — Elcam Medical Italy SPA

Elcam Medical Italy SPA — FEI 3004960482

The FDA completed an inspection of Elcam Medical Italy SPA on July 9, 2009 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
July 9, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Carpi (Italy)