FDA Inspection 1266787 — Michael D. Greenwood, MD

Michael D. Greenwood, MD — FEI 3035147014

The FDA completed an inspection of Michael D. Greenwood, MD on April 11, 2025 in West Fargo, ND. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
West Fargo, ND (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
296821 CFR 812.100Investigator non-compliance with agreement/plan/regulations