FDA Inspection 836382 — GC America, Inc.

GC America, Inc. — FEI 1410097

The FDA completed an inspection of GC America, Inc. on June 13, 2013 in Alsip, IL. 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
June 13, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Alsip, IL (United States)