# FDA Inspection 900723 - Suvranu Ganguli, MD - October 17, 2014

Source: https://www.keypedia.com/records/fda_inspections/suvranu-ganguli-md/c2786af0-1ad2-4c6a-8dc0-d06f5bfac182
Source feed: FDA_Inspections

> FDA Inspection 900723 for Suvranu Ganguli, MD on October 17, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900723
- Company Name: Suvranu Ganguli, MD
- Inspection Date: 2014-10-17
- 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/suvranu-ganguli-md/c89641fc-19cf-48c3-9d40-33ccf801a4a0

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