FDA Inspection 1221235 — Wayne M. Clark, MD

Wayne M. Clark, MD — FEI 3008154173

The FDA completed an inspection of Wayne M. Clark, MD on Oct 27, 2023 in Portland, OR. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 27, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Portland, OR (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations

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