# FDA Inspection 1052173 - Wondfo USA Co Ltd - May 11, 2018

Source: https://www.keypedia.com/records/fda_inspections/wondfo-usa-co-ltd/85d2571d-dfab-4a91-8a7e-eaf9a7688b8f
Source feed: FDA_Inspections

> FDA Inspection 1052173 for Wondfo USA Co Ltd on May 11, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1052173
- Company Name: Wondfo USA Co Ltd
- Inspection Date: 2018-05-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1052173 - 2018-05-11](https://www.keypedia.com/records/fda_inspections/wondfo-usa-co-ltd/a858a3a4-b91e-4983-b9bd-0c58a9c22aac)

Company: https://www.keypedia.com/companies/wondfo-usa-co-ltd/3e25dba4-8b88-43a8-9aa7-2802e7f602c4

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