FDA Inspection 1234038 — Janaki (NMI) Nadarajah DPM

Janaki (NMI) Nadarajah DPM — FEI 3009064394

The FDA completed an inspection of Janaki (NMI) Nadarajah DPM on Mar 7, 2024 in Augusta, GA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Mar 7, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Augusta, GA (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
752621 CFR 312.62(a)Accountability records
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance