FDA Inspection 938933 — XZeal Technologies, Inc.
The FDA completed an inspection of XZeal Technologies, Inc. on August 19, 2015 in Kissimmee, FL. 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
- August 19, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Kissimmee, FL (United States)