FDA Inspection 1299594 — YiChang HEC ChangJiang Pharmaceutical Co., Ltd.
The FDA completed an inspection of YiChang HEC ChangJiang Pharmaceutical Co., Ltd. on Oct 30, 2025 in Yidu. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 30, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Yidu (China)