FDA Inspection 926321 — Anbotek Compliance Laboratory Ltd.
The FDA completed an inspection of Anbotek Compliance Laboratory Ltd. on November 6, 2014 in Shenzhen. 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
- November 6, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Shenzhen (China)