FDA Inspection 576565 — Mark V. DiBuono, MD

Mark V. DiBuono, MD — FEI 3007159391

The FDA completed an inspection of Mark V. DiBuono, MD on Dec 22, 2008 in Staten Island, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 22, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Staten Island, NY (United States)

Additional Details

Clinical Investigator (CI)