# FDA Inspection 780529 - SHENZHEN KINGYIELD TECHNOLOGY CO., LTD - May 04, 2012

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-kingyield-technology-co-ltd/970967f7-e83d-4a4a-9962-801a2b6d86cc
Source feed: FDA_Inspections

> FDA Inspection 780529 for SHENZHEN KINGYIELD TECHNOLOGY CO., LTD on May 04, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 780529
- Company Name: SHENZHEN KINGYIELD TECHNOLOGY CO., LTD
- Inspection Date: 2012-05-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [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