# FDA Inspection 1112304 - Susheel Kodali, M.D. - November 20, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/susheel-kodali-md/bb0c6241-8639-4818-9166-5283d9fcbc6a
Source feed: FDA_Inspections

> FDA Inspection 1112304 for Susheel Kodali, M.D. on November 20, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1112304
- Company Name: Susheel Kodali, M.D.
- Inspection Date: 2019-11-20
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1293354 - 2025-11-26](https://www.globalkeysolutions.net/records/fda_inspections/susheel-kodali-md/db46e525-3f16-415a-9373-650fe2747792)
- [FDA Inspection 1293354 - 2025-11-26](https://www.globalkeysolutions.net/records/fda_inspections/susheel-kodali-md/28d14a68-8aa6-4914-a4e9-b7f22f58d0ca)
- [FDA Inspection 816801 - 2013-01-31](https://www.globalkeysolutions.net/records/fda_inspections/susheel-kodali-md/027328a9-ce8e-4b74-a977-9661ec13d96d)

Company: https://www.globalkeysolutions.net/companies/susheel-kodali-md/c44af65c-0d10-41a4-aaa8-3ba67ce6ab2a

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