# Stefan W. Kreuzer, MD – FDA Inspection, Aug 13, 2019

Source: https://www.keypedia.com/records/fda_inspections/stefan-w-kreuzer-md/6e0ecffa-ef58-4ed7-986f-9cd3c365e29a
Source feed: FDA_Inspections

> FDA inspection 1099416 of Stefan W. Kreuzer, MD, August 13, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1099416
- Company Name: Stefan W. Kreuzer, MD
- Inspection Date: 2019-08-13
- 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: 1

## Related Documents

- FDA Inspection 823260 - 2013-03-08

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/anya-d-lockett-evans/afddc255-78ab-472c-9a69-f4cb9967f180)

Company: https://www.keypedia.com/companies/stefan-w-kreuzer-md/9a806cb8-a3f1-4c80-bacf-d16a4690635b

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