# FDA Inspection 885238 - Ramesh Hariharan, MD - June 17, 2014

Source: https://www.keypedia.com/records/fda_inspections/ramesh-hariharan-md/c0f2604a-f04c-42dc-8455-8f660129d806
Source feed: FDA_Inspections

> FDA Inspection 885238 for Ramesh Hariharan, MD on June 17, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 885238
- Company Name: Ramesh Hariharan, MD
- Inspection Date: 2014-06-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1141316 - 2021-04-09](https://www.keypedia.com/records/fda_inspections/ramesh-hariharan-md/9821dc75-8704-4f62-8bfc-f8f179e5aafb)

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