FDA Inspection 1204113 — Fayz A. Hudefi, M.D.

Fayz A. Hudefi, M.D. — FEI 3016580854

The FDA completed an inspection of Fayz A. Hudefi, M.D. on Apr 21, 2023 in Bentonville, AR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 21, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Bentonville, AR (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
2272821 CFR 312.64(b)Safety Reports - Non-Serious Events
756021 CFR 312.60FD-1572, protocol compliance

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