FDA Inspection 1100379 — Ronald F. Tutrone, Jr., MD

Ronald F. Tutrone, Jr., MD — FEI 3000207122

The FDA completed an inspection of Ronald F. Tutrone, Jr., MD on August 16, 2019 in Towson, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Towson, MD (United States)

Additional Details

Clinical Investigator (CI)