# FDA Inspection 1177840 - Sunil S. Dhawan, MD - August 05, 2022

Source: https://www.keypedia.com/records/fda_inspections/sunil-s-dhawan-md/9bfb59dd-8e89-4543-94c6-3cd8780111e8
Source feed: FDA_Inspections

> FDA Inspection 1177840 for Sunil S. Dhawan, MD on August 05, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1177840
- Company Name: Sunil S. Dhawan, MD
- Inspection Date: 2022-08-05
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 922401 - 2015-04-14](https://www.keypedia.com/records/fda_inspections/sunil-s-dhawan-md/6865b83f-0c01-4448-b20e-bf83aa9cd1ac)
- [FDA Inspection 672849 - 2010-07-14](https://www.keypedia.com/records/fda_inspections/sunil-s-dhawan-md/ac2125fc-6db9-4f75-88f7-2252d03bc99d)

Company: https://www.keypedia.com/companies/sunil-s-dhawan-md/5ad0ff3b-a312-43dc-abfc-d6078c299723

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