# Mark S. Slaughter MD – FDA Inspection, May 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/mark-s-slaughter-md/ef80a99c-c70f-4aa9-b471-c3da531ce1a1
Source feed: FDA_Inspections

> FDA inspection 1011489 of Mark S. Slaughter MD, May 02, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1011489
- Company Name: Mark S. Slaughter MD
- Inspection Date: 2017-05-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 697315 - 2010-11-08

## Related Officers

- [Company Rep](https://www.keypedia.com/people/karen-m-cooper/4813e60d-c8da-4df2-bc48-ecfb06a55cf8)

Company: https://www.keypedia.com/companies/mark-s-slaughter-md/0224af28-284b-4853-9499-32ed731ca18d

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