# FDA Inspection 1141316 - Ramesh Hariharan, MD - April 09, 2021

Source: https://www.keypedia.com/records/fda_inspections/ramesh-hariharan-md/9821dc75-8704-4f62-8bfc-f8f179e5aafb
Source feed: FDA_Inspections

> FDA Inspection 1141316 for Ramesh Hariharan, MD on April 09, 2021. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1141316
- Company Name: Ramesh Hariharan, MD
- Inspection Date: 2021-04-09
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 885238 - 2014-06-17](https://www.keypedia.com/records/fda_inspections/ramesh-hariharan-md/c0f2604a-f04c-42dc-8455-8f660129d806)

Company: https://www.keypedia.com/companies/ramesh-hariharan-md/096c4e1a-44ff-4bcb-a09c-9804e2152c03

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