FDA Inspection 825866 — iCRco, Inc.

iCRco, Inc. — FEI 3009717300

The FDA completed an inspection of iCRco, Inc. on Mar 28, 2013 in Goleta, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 28, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Goleta, CA (United States)