FDA Inspection 1328354 — Miha Bodytec Inc

Miha Bodytec Inc — FEI 3015529344

The FDA completed an inspection of Miha Bodytec Inc on Jun 17, 2026 in Addison, 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 17, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Addison, IL (United States)