FDA Inspection 1197006 — Madeleine Duvic, M.D.

Madeleine Duvic, M.D. — FEI 3007037118

The FDA completed an inspection of Madeleine Duvic, M.D. on January 13, 2023 in Houston, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 13, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Houston, TX (United States)

Additional Details

Clinical Investigator (CI)