# Ramesh Hariharan, MD – FDA Inspection, Jun 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 of Ramesh Hariharan, MD, June 17, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1141316 - 2021-04-09

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