FDA Inspection 1018296 — Suzanne Groah, MD

Suzanne Groah, MD — FEI 3013119695

The FDA completed an inspection of Suzanne Groah, MD on April 4, 2017 in Washington, DC. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 4, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Washington, DC (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
755221 CFR 312.66Changes in research
763221 CFR 312.6(a)Required label statement