FDA Inspection 1056979 — Anhui Kangda Medical Products Co., Ltd.
The FDA completed an inspection of Anhui Kangda Medical Products Co., Ltd. on June 13, 2018 in Chuzhou. 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
- June 13, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Chuzhou (China)