FDA Inspection 995178 — Neelima Denduluri, MD

Neelima Denduluri, MD — FEI 3013077354

The FDA completed an inspection of Neelima Denduluri, MD on Dec 6, 2016 in Fairfax, VA. 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
Dec 6, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Fairfax, VA (United States)

Additional Details

Clinical Investigator (CI)

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