# Vincent L. Rowe, MD – FDA Inspection, Jul 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/vincent-l-rowe-md/bc42596b-c0f0-4594-837f-91c5fa586471
Source feed: FDA_Inspections

> FDA inspection 1019482 of Vincent L. Rowe, MD, July 28, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019482
- Company Name: Vincent L. Rowe, MD
- Inspection Date: 2017-07-28
- 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

- [Issuing Officer](https://www.keypedia.com/people/dawn-c-olenjack/b5a18d10-cd4b-405e-9016-8f5274a33000)

Company: https://www.keypedia.com/companies/vincent-l-rowe-md/bc29637f-dd75-4d4b-a9e0-a098abaa66fc

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