FDA Inspection 830427 — iCAD, INC.

iCAD, INC. — FEI 3026970882

The FDA completed an inspection of iCAD, INC. on May 7, 2013 in Nashua, NH. 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
May 7, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Nashua, NH (United States)