# FDA Inspection 1276531 - Jiangxi Sanxin MedTec Co., Ltd. - June 25, 2025

Source: https://www.keypedia.com/records/fda_inspections/jiangxi-sanxin-medtec-co-ltd/49c9ef92-d11f-4e2a-8c58-2c574fb33a38
Source feed: FDA_Inspections

> FDA Inspection 1276531 for Jiangxi Sanxin MedTec Co., Ltd. on June 25, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276531
- Company Name: Jiangxi Sanxin MedTec Co., Ltd.
- Inspection Date: 2025-06-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276531 - 2025-06-25](https://www.keypedia.com/records/fda_inspections/jiangxi-sanxin-medtec-co-ltd/c999e402-9c68-4752-8ea8-2e07e97a6508)
- [FDA Inspection 890434 - 2014-07-31](https://www.keypedia.com/records/fda_inspections/jiangxi-sanxin-medtec-co-ltd/6644aa12-e201-4866-989b-5f6ca5dab885)

Company: https://www.keypedia.com/companies/jiangxi-sanxin-medtec-co-ltd/4e302f75-ba6a-4fa8-b937-26437e992fbd

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