# FDA Inspection 982307 - Shenzhen Qiaohua Industries Limited - June 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-qiaohua-industries-limited/5c8cebde-3d2c-4780-bed3-76fd9c1cd912
Source feed: FDA_Inspections

> FDA Inspection 982307 for Shenzhen Qiaohua Industries Limited on June 07, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 982307
- Company Name: Shenzhen Qiaohua Industries Limited
- Inspection Date: 2016-06-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 803255 - 2012-07-27](https://www.keypedia.com/records/fda_inspections/shenzhen-qiaohua-industries-limited/1e9c083d-7773-45c2-b25d-74aba0514d91)

Company: https://www.keypedia.com/companies/shenzhen-qiaohua-industries-limited/2c8380e2-5b79-492f-87b0-fa84a1531a31

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