# James Warner Genuario, MD – FDA Inspection, Dec 6, 2018

Source: https://www.keypedia.com/records/fda_inspections/james-warner-genuario-md/737f0659-ed7c-4446-b660-4c9fc6ca0cf7
Source feed: FDA_Inspections

> FDA inspection 1073982 of James Warner Genuario, MD, December 06, 2018. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073982
- Company Name: James Warner Genuario, MD
- Inspection Date: 2018-12-06
- 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: 5

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/theressa-b-smith/80f0c339-7eac-4c73-b9f6-ecb368738fe6)

Company: https://www.keypedia.com/companies/james-warner-genuario-md/d8e440f1-1e8e-4871-93b8-91c7bfc275ef

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