FDA Inspection 942440 — Columbus Canvas Products

Columbus Canvas Products — FEI 3009410520

The FDA completed an inspection of Columbus Canvas Products on September 15, 2015 in Columbus, OH. 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
September 15, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)