FDA Inspection 1272098 — Stephen J. Monteith, MD

Stephen J. Monteith, MD — FEI 3025534971

The FDA completed an inspection of Stephen J. Monteith, MD on June 9, 2025 in Seattle, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 9, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Seattle, WA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations