FDA Inspection 1271048 — C-Axis Inc.

C-Axis Inc. — FEI 3004016606

The FDA completed an inspection of C-Axis Inc. on April 30, 2025 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
April 30, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Hamel, MN (United States)