FDA Inspection 817134 — iMed Technology, Inc
The FDA completed an inspection of iMed Technology, Inc on Jan 30, 2013 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
- Jan 30, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Mckinney, TX (United States)