# FDA Inspection 921904 - SHENZHEN KINGYIELD TECHNOLOGY CO., LTD - March 05, 2015

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-kingyield-technology-co-ltd/9f5167f5-424f-4a61-996e-78140852cea1
Source feed: FDA_Inspections

> FDA Inspection 921904 for SHENZHEN KINGYIELD TECHNOLOGY CO., LTD on March 05, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 921904
- Company Name: SHENZHEN KINGYIELD TECHNOLOGY CO., LTD
- Inspection Date: 2015-03-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 780529 - 2012-05-04](https://www.keypedia.com/records/fda_inspections/shenzhen-kingyield-technology-co-ltd/970967f7-e83d-4a4a-9962-801a2b6d86cc)
- [FDA Inspection 780529 - 2012-05-04](https://www.keypedia.com/records/fda_inspections/shenzhen-kingyield-technology-co-ltd/c543a687-11f8-4dd8-94dc-a38928ee49fd)

Company: https://www.keypedia.com/companies/shenzhen-kingyield-technology-co-ltd/32822f59-8c88-4a30-8c73-f3e75639d902

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