FDA Inspection 930311 — ABS Corp

ABS Corp — FEI 3002675394

The FDA completed an inspection of ABS Corp on June 9, 2015 in Minnetonka, MN. 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
June 9, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)