FDA Inspection 1105956 — Columbus Canvas Products

Columbus Canvas Products — FEI 3009410520

The FDA completed an inspection of Columbus Canvas Products on September 25, 2019 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 25, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)