FDA Inspection 1062853 — AMS S.r.l.

AMS S.r.l. — FEI 3005150500

The FDA completed an inspection of AMS S.r.l. on July 26, 2018 in Guidonia Montecelio. 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 26, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Guidonia Montecelio (Italy)