FDA Inspection 1066596 — Ajex Meditech Ltd
The FDA completed an inspection of Ajex Meditech Ltd on July 12, 2018 in Suwon. 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 12, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Suwon (Korea (the Republic of))