FDA Inspection 1326458 — 3DPX Medical

3DPX Medical — FEI 3017567754

The FDA completed an inspection of 3DPX Medical on Jun 22, 2026 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 22, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Chicago, IL (United States)