# FDA Inspection 1279097 - TIANJIN RILIFINE MEDICAL DEVICE CO LTD - July 31, 2025

Source: https://www.keypedia.com/records/fda_inspections/tianjin-rilifine-medical-device-co-ltd/112dcf52-3893-462f-bc4d-2b4c1780c595
Source feed: FDA_Inspections

> FDA Inspection 1279097 for TIANJIN RILIFINE MEDICAL DEVICE CO LTD on July 31, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279097
- Company Name: TIANJIN RILIFINE MEDICAL DEVICE CO LTD
- Inspection Date: 2025-07-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1279097 - 2025-07-31](https://www.keypedia.com/records/fda_inspections/tianjin-rilifine-medical-device-co-ltd/8c0d5e4b-fdec-40ba-98ab-55cd2aef36ed)
- [FDA Inspection 1279097 - 2025-07-31](https://www.keypedia.com/records/fda_inspections/tianjin-rilifine-medical-device-co-ltd/0a105ac6-d441-478c-bd8c-7586405f6e90)

Company: https://www.keypedia.com/companies/tianjin-rilifine-medical-device-co-ltd/12de6514-a2c6-4cb1-a6b4-8666b3c2804a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7