# FDA Inspection 831941 - Santosh Kesari, M.D. - May 03, 2013

Source: https://www.keypedia.com/records/fda_inspections/santosh-kesari-md/26fdabfe-88c2-412d-9dd5-fb08ed08f555
Source feed: FDA_Inspections

> FDA Inspection 831941 for Santosh Kesari, M.D. on May 03, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 831941
- Company Name: Santosh Kesari, M.D.
- Inspection Date: 2013-05-03
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/santosh-kesari-md/5d037e13-16b0-4166-bd55-c128011ab135

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