# Khosla, Sundeep, MD – FDA Inspection, Dec 7, 2018

Source: https://www.keypedia.com/records/fda_inspections/khosla-sundeep-md/f73c7168-d05f-454a-a2ee-4d4c98eb0f75
Source feed: FDA_Inspections

> FDA inspection 1073960 of Khosla, Sundeep, MD, December 07, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073960
- Company Name: Khosla, Sundeep, MD
- Inspection Date: 2018-12-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/kellie-l-thommes/255a1b92-cd56-41f5-9622-82e8a629e153)

Company: https://www.keypedia.com/companies/khosla-sundeep-md/89489063-ab95-412c-bea1-d75969ee958c

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