FDA Inspection 1299594 — YiChang HEC ChangJiang Pharmaceutical Co., Ltd.
The FDA completed an inspection of YiChang HEC ChangJiang Pharmaceutical Co., Ltd. on October 30, 2025 in Yidu. 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
- October 30, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Yidu (China)