FDA Inspection 1068402 — Stephen Huddleston MD

Stephen Huddleston MD — FEI 3014721746

The FDA completed an inspection of Stephen Huddleston MD on Oct 11, 2018 in Minneapolis, MN. 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 11, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate
1450821 CFR 812.140(a)(4)Investigator record of protocol deviations inadequate
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations