FDA Inspection 1281081 — Deirdre O. Hooper, M.D.

Deirdre O. Hooper, M.D. — FEI 3015729047

The FDA completed an inspection of Deirdre O. Hooper, M.D. on September 10, 2025 in New Orleans, LA. 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
September 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
New Orleans, LA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
1450521 CFR 812.140(a)(3)Investigator's subject records inadequate