FDA Inspection 1050476 — Roberto Salvatori, M.D.

Roberto Salvatori, M.D. — FEI 3010647690

The FDA completed an inspection of Roberto Salvatori, M.D. on April 24, 2018 in Baltimore, MD. 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
April 24, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)