# FDA Inspection 598989 - Mandeep S. Oberoi, M.D. - July 24, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/mandeep-s-oberoi-md/9eb773ea-9a34-4a28-94a6-a3bc4897d4e6
Source feed: FDA_Inspections

> FDA Inspection 598989 for Mandeep S. Oberoi, M.D. on July 24, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 598989
- Company Name: Mandeep S. Oberoi, M.D.
- Inspection Date: 2009-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1114971 - 2020-01-10](https://www.globalkeysolutions.net/records/fda_inspections/mandeep-s-oberoi-md/92a87cc5-5167-4e34-9f8d-d3f6a15ba6df)
- [FDA Inspection 890725 - 2014-08-01](https://www.globalkeysolutions.net/records/fda_inspections/mandeep-s-oberoi-md/9c67daf0-6c67-4e28-bca6-68fab3e3f6c1)
- [FDA Inspection 542788 - 2008-10-21](https://www.globalkeysolutions.net/records/fda_inspections/mandeep-s-oberoi-md/61288636-3a3c-46bf-b2be-d014d6c80aa8)

Company: https://www.globalkeysolutions.net/companies/mandeep-s-oberoi-md/4bac5b7b-c63f-4bf6-b135-46d1364e0704

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