# FDA Inspection 1073960 - Khosla, Sundeep, MD - December 07, 2018

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

> FDA Inspection 1073960 for Khosla, Sundeep, MD on December 07, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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