Steve E. Canfield, M.D. – FDA Inspection, Nov 27, 2024

Record Details

This FDA Inspection record concerns Steve E. Canfield, M.D., with an inspection on November 27, 2024, issued by the Dallas District Office, covering medical devices & rad health.

Company: Steve E. Canfield, M.D.
Inspection Date: November 27, 2024
Product Type: Medical Devices & Rad Health
Office: Dallas District Office
Person: Andrea A. Branche (FDA Associated Person)

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ID · 5c1ded54-e0eb-417b-82fa-0436173aa1e9

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number: 1255226
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
21 CFR 812.110(d)Inadequate financial disclosure by investigator

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FDA Inspection

Steve E. Canfield, M.D.November 27, 2024