FDA Inspection 800717 — AMS (US) Inc.

AMS (US) Inc. — FEI 3008450080

The FDA completed an inspection of AMS (US) Inc. on September 26, 2012 in Norwell, MA. 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
September 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Norwell, MA (United States)