FDA Inspection 938632 — Hyperion Medical Technologies Inc
The FDA completed an inspection of Hyperion Medical Technologies Inc on July 9, 2015 in Addison, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 9, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Addison, TX (United States)