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Eli Lilly And Company

⚠️ High Risk

FEI: 3012344499 • Indianapolis, IN • UNITED STATES

FEI

FEI Number

3012344499

📍

Location

Indianapolis, IN

🇺🇸
🏢

Address

639 S Delaware St, , Indianapolis, IN, United States

High Risk

FDA Import Risk Assessment

58.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
5/7/2025
Latest Refusal
9/11/2023
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
71.3×20%
Frequency
18.1×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
5/7/2025
61PDK74TIRZEPATIDE (ANTI-DIABETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/1/2025
61PCK74TIRZEPATIDE (ANTI-DIABETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/11/2023
61NCA66FLUOXETINE HYDROCHLORIDE (ANTI-DEPRESSANT)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Eli Lilly And Company's FDA import refusal history?

Eli Lilly And Company (FEI: 3012344499) has 3 FDA import refusal record(s) in our database, spanning from 9/11/2023 to 5/7/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Eli Lilly And Company's FEI number is 3012344499.

What types of violations has Eli Lilly And Company received?

Eli Lilly And Company has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Eli Lilly And Company come from?

All FDA import refusal data for Eli Lilly And Company is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.