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

Record Details

This FDA Inspection record concerns Ken Y. Yoneda, M.D., with an inspection on December 6, 2024, issued by the San Francisco District Office, covering medical devices & rad health.

Company: Ken Y. Yoneda, M.D.
Inspection Date: December 6, 2024
Product Type: Medical Devices & Rad Health
Office: San Francisco District Office
Person: Stephanie Barragan (Company Rep)

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ID · cf684397-469c-4466-a5e9-c555742eb670

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number: 1255891
FDA center: Medical Devices & Rad Health
Project area: Product Evaluation: Medical Devices
Outcome: Form 483 issued, view the record

FDA Citations

21 CFR 812.100Investigator non-compliance with agreement/plan/regulations

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FDA Inspection

Ken Y. Yoneda, M.D.December 6, 2024