FDA Inspection 1049249 — iCRco, Inc.

iCRco, Inc. — FEI 3009717300

The FDA completed an inspection of iCRco, Inc. on Apr 20, 2018 in Goleta, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 20, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Goleta, CA (United States)