FDA Inspection 1153399 — Alexandra Rogers, MD

Alexandra Rogers, MD — FEI 3020036689

The FDA completed an inspection of Alexandra Rogers, MD on October 1, 2021 in Santa Barbara, CA. 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
October 1, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Santa Barbara, CA (United States)

Additional Details

Clinical Investigator (CI)

Citations

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