FDA Inspection 1279425 — iMed Technology, Inc

iMed Technology, Inc — FEI 3003813437

The FDA completed an inspection of iMed Technology, Inc on August 6, 2025 in Mckinney, TX. 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
August 6, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Mckinney, TX (United States)