FDA Inspection 1009761 — ACI, Inc.

ACI, Inc. — FEI 3005863177

The FDA completed an inspection of ACI, Inc. on April 26, 2017 in Overland Park, KS. 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
April 26, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Overland Park, KS (United States)