FDA Inspection 1028867 — Saumya Sharma, MD

Saumya Sharma, MD — FEI 3013846043

The FDA completed an inspection of Saumya Sharma, MD on Oct 18, 2017 in Houston, TX. 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.