FDA Inspection 1014455 — iMed Technology, Inc
The FDA completed an inspection of iMed Technology, Inc on Jun 16, 2017 in Mckinney, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 16, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Mckinney, TX (United States)