# FDA Inspection 980981 - Huijian Wang, MD - July 19, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/huijian-wang-md/da383ce2-5bd7-496b-9a58-628becb0c21f
Source feed: FDA_Inspections

> FDA Inspection 980981 for Huijian Wang, MD on July 19, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980981
- Company Name: Huijian Wang, MD
- Inspection Date: 2016-07-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/huijian-wang-md/3639e048-70a4-400e-ac60-ec983b98e0c1

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