# Thomas Sutton, MD – FDA Inspection, May 7, 2018

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

> FDA inspection 1050996 of Thomas Sutton, MD, May 07, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 812. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1050996
- Company Name: Thomas Sutton, MD
- Inspection Date: 2018-05-07
- 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: 3

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-t-hansen/7ae1f1df-7f68-4264-bd87-ea21c8d879bb)
- [Company Rep](https://www.keypedia.com/people/vickie-j-kanion/4ec38844-d90f-490e-bdfb-7bcee20fcc90)

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