# Saumya Sharma, MD – FDA Inspection, Oct 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/saumya-sharma-md/b8a038ee-a923-43f0-a6e9-58b484d7702f
Source feed: FDA_Inspections

> FDA inspection 1028867 of Saumya Sharma, MD, October 18, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1028867
- Company Name: Saumya Sharma, MD
- Inspection Date: 2017-10-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1197609 - 2023-02-03

## Related Officers

- [Company Rep](https://www.keypedia.com/people/leighton-k-ngai/39fc01c8-e40a-45d4-910a-068955d16a06)

Company: https://www.keypedia.com/companies/saumya-sharma-md/24ce5784-9fc8-4258-8c95-5a356b834264

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