FDA Inspection 1037479 — De Gotzen S.R.L.

De Gotzen S.R.L. — FEI 3002994636

The FDA completed an inspection of De Gotzen S.R.L. on Dec 21, 2017 in Olgiate Olona. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 21, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Olgiate Olona (Italy)