FDA Inspection 974218 — CliniComp International Inc

CliniComp International Inc — FEI 1000142646

The FDA completed an inspection of CliniComp International Inc on June 17, 2016 in San Diego, CA. 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 17, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)