FDA Inspection 1279425 — iMed Technology, Inc

iMed Technology, Inc — FEI 3003813437

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.