FDA Inspection 1256510 — Tim Smith, M.D.

Tim Smith, M.D. — FEI 3031869799

The FDA completed an inspection of Tim Smith, M.D. on Dec 10, 2024 in Cincinnati, OH. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 10, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Cincinnati, OH (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations

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