# Kevin T. Lavery, MD – FDA Inspection, Mar 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/kevin-t-lavery-md/db583d34-112b-48fc-93f2-3ebe5cf6e356
Source feed: FDA_Inspections

> FDA inspection 1046240 of Kevin T. Lavery, MD, March 29, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046240
- Company Name: Kevin T. Lavery, MD
- Inspection Date: 2018-03-29
- 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 Officers

- [FDA Associated Person](https://www.keypedia.com/people/andrace-deyampert/cdb4f833-488b-42b9-abab-4216435bce4c)

Company: https://www.keypedia.com/companies/kevin-t-lavery-md/2c096585-3a99-4226-99b0-26c1819f3561

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