FDA Inspection 1229895 — Eli Lilly & Company

Eli Lilly & Company — FEI 1819470

The FDA completed an inspection of Eli Lilly & Company on January 15, 2025 in Indianapolis, IN. 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
January 15, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Indianapolis, IN (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)