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