FDA Inspection 980981 — Huijian Wang, MD

Huijian Wang, MD — FEI 3012286005

The FDA completed an inspection of Huijian Wang, MD on Jul 19, 2016 in Daytona Beach, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.