FDA Inspection 919865 — ARC Medical Inc.

ARC Medical Inc. — FEI 1000111925

The FDA completed an inspection of ARC Medical Inc. on February 26, 2015 in Tucker, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 26, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Tucker, GA (United States)