# Wondfo USA Co Ltd – FDA Inspection, May 11, 2018

Source: https://www.keypedia.com/records/fda_inspections/wondfo-usa-co-ltd/a858a3a4-b91e-4983-b9bd-0c58a9c22aac
Source feed: FDA_Inspections

> FDA inspection 1052173 of Wondfo USA Co Ltd, May 11, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1052173
- Company Name: Wondfo USA Co Ltd
- Inspection Date: 2018-05-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

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