# FDA Inspection 877770 - Guangzhou Wondfo Biotech Co., Ltd. - April 11, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/guangzhou-wondfo-biotech-co-ltd/20813c39-46ac-4ff6-b1b6-6e19e426f943
Source feed: FDA_Inspections

> FDA Inspection 877770 for Guangzhou Wondfo Biotech Co., Ltd. on April 11, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 877770
- Company Name: Guangzhou Wondfo Biotech Co., Ltd.
- Inspection Date: 2014-04-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 877770 - 2014-04-11](https://www.globalkeysolutions.net/records/fda_inspections/guangzhou-wondfo-biotech-co-ltd/de290973-162d-45d6-a9ca-fc7fd56b74f5)
- [FDA Inspection 575291 - 2009-03-27](https://www.globalkeysolutions.net/records/fda_inspections/guangzhou-wondfo-biotech-co-ltd/97475c23-5a43-4909-83fe-93b3d5db8187)

Company: https://www.globalkeysolutions.net/companies/guangzhou-wondfo-biotech-co-ltd/f821880b-103a-41bf-aebe-4b31ec7e9a9e

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