# FDA Inspection 1050996 - Thomas Sutton, MD - May 07, 2018

Source: https://www.keypedia.com/records/fda_inspections/thomas-sutton-md/6fd524a6-e196-4c80-93de-dd2e978d79b0
Source feed: FDA_Inspections

> FDA Inspection 1050996 for Thomas Sutton, MD on May 07, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050996
- Company Name: Thomas Sutton, MD
- Inspection Date: 2018-05-07
- 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/thomas-sutton-md/866c32ba-5d78-4be2-ac5c-6ccfc3b721ad

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