# FDA Inspection 1029014 - Taicang Kanghui Technology Development Company, Ltd. - September 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/taicang-kanghui-technology-development-company-ltd/583ad9ea-4d49-4510-be1e-9e5a04d41ca6
Source feed: FDA_Inspections

> FDA Inspection 1029014 for Taicang Kanghui Technology Development Company, Ltd. on September 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029014
- Company Name: Taicang Kanghui Technology Development Company, Ltd.
- Inspection Date: 2017-09-21
- 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 1029014 - 2017-09-21](https://www.keypedia.com/records/fda_inspections/taicang-kanghui-technology-development-company-ltd/239d22b7-a24a-460f-9d53-d164dd54a6be)
- [FDA Inspection 884269 - 2014-05-21](https://www.keypedia.com/records/fda_inspections/taicang-kanghui-technology-development-company-ltd/cd0e175c-7853-401b-833d-e451401a0b4d)

Company: https://www.keypedia.com/companies/taicang-kanghui-technology-development-company-ltd/67b9ebe9-485f-4d1a-8579-5bbc76f02a21

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