FDA Inspection 1264670 — Anupama Nehra, M.D.

Anupama Nehra, M.D. — FEI 3035385117

The FDA completed an inspection of Anupama Nehra, M.D. on March 24, 2025 in Newark, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 24, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Newark, NJ (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate
753121 CFR 312.62(c)Record retention
756021 CFR 312.60FD-1572, protocol compliance