FDA Inspection 1279097 — TIANJIN RILIFINE MEDICAL DEVICE CO LTD
The FDA completed an inspection of TIANJIN RILIFINE MEDICAL DEVICE CO LTD on July 31, 2025 in Tianjin. 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 31, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tianjin (China)