# FDA Inspection 889472 - CHANGSHUSHI BOYI MEDICAL DEVICE CO., LTD. - July 30, 2014

Source: https://www.keypedia.com/records/fda_inspections/changshushi-boyi-medical-device-co-ltd/30860a39-3ba3-47ab-b75a-7c5dcdcff1fd
Source feed: FDA_Inspections

> FDA Inspection 889472 for CHANGSHUSHI BOYI MEDICAL DEVICE CO., LTD. on July 30, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 889472
- Company Name: CHANGSHUSHI BOYI MEDICAL DEVICE CO., LTD.
- Inspection Date: 2014-07-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 889472 - 2014-07-30](https://www.keypedia.com/records/fda_inspections/changshushi-boyi-medical-device-co-ltd/ab51cc96-3672-4093-9122-8cd31a39369a)

Company: https://www.keypedia.com/companies/changshushi-boyi-medical-device-co-ltd/11da1460-c9d5-4ac7-b9fb-d0c1cae4e85a

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