# FDA Inspection 804840 - Suresh Neelagaru, MD - October 19, 2012

Source: https://www.keypedia.com/records/fda_inspections/suresh-neelagaru-md/9290be7d-5c78-4adf-8c82-335ddaa7e091
Source feed: FDA_Inspections

> FDA Inspection 804840 for Suresh Neelagaru, MD on October 19, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 804840
- Company Name: Suresh Neelagaru, MD
- Inspection Date: 2012-10-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/suresh-neelagaru-md/e90c537a-385c-48d7-b4f5-b6c4ce175bd3

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