FDA Inspection 1071552 — Preeti Raghavan, M.D.

Preeti Raghavan, M.D. — FEI 3014731892

The FDA completed an inspection of Preeti Raghavan, M.D. on Oct 16, 2018 in New York, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 16, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
New York, NY (United States)

Additional Details

Clinical Investigator (CI)

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