# Ken Y. Yoneda, M.D. – FDA Inspection, Dec 6, 2024

Source: https://www.keypedia.com/records/fda_inspections/ken-y-yoneda-md/cf684397-469c-4466-a5e9-c555742eb670
Source feed: FDA_Inspections

> FDA inspection 1255891 of Ken Y. Yoneda, M.D., December 06, 2024. 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: 1255891
- Company Name: Ken Y. Yoneda, M.D.
- Inspection Date: 2024-12-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: San Francisco District Office
- Citation Count: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephanie-barragan/fc1bc901-1467-4fdd-bee3-f87f2db3a1fa)

Company: https://www.keypedia.com/companies/ken-y-yoneda-md/501d2ed6-38a9-417b-ba7c-19b04284646e

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