FDA Inspection 806217 — Sunil Verma, M.D.

Sunil Verma, M.D. — FEI 3009751999

The FDA completed an inspection of Sunil Verma, M.D. on November 2, 2012 in Toronto. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 2, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Toronto (Canada)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate