FDA Inspection 913223 — IMRIS Imaging Inc

IMRIS Imaging Inc — FEI 3010326005

The FDA completed an inspection of IMRIS Imaging Inc on February 4, 2015 in Chaska, MN. 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
February 4, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Chaska, MN (United States)