FDA Inspection 746032 — C-Axis Inc.

C-Axis Inc. — FEI 3004016606

The FDA completed an inspection of C-Axis Inc. on September 21, 2011 in Hamel, 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
September 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Hamel, MN (United States)