FDA Inspection 835249 — AcQPoint, Inc

AcQPoint, Inc — FEI 3008828227

The FDA completed an inspection of AcQPoint, Inc on June 4, 2013 in La Quinta, 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 4, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
La Quinta, CA (United States)