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Eli Lilly & Co

⚠️ High Risk

FEI: 3009963246 • Indianapolis, IN • UNITED STATES

FEI

FEI Number

3009963246

📍

Location

Indianapolis, IN

🇺🇸
🏢

Address

355 E Merrill St, , Indianapolis, IN, United States

High Risk

FDA Import Risk Assessment

53.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
7/23/2025
Latest Refusal
10/1/2024
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
17.7×30%
Recency
75.8×20%
Frequency
20.0×10%
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

752×

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).

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

Refusal History

DateProductViolationsDivision
7/23/2025
61PDY17INSULIN (INJ) (ANTI-DIABETIC)
118NOT LISTED
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/1/2024
61PCL74TIRZEPATIDE (ANTI-DIABETIC)
75UNAPPROVED
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Eli Lilly & Co's FDA import refusal history?

Eli Lilly & Co (FEI: 3009963246) has 2 FDA import refusal record(s) in our database, spanning from 10/1/2024 to 7/23/2025.

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 & Co's FEI number is 3009963246.

What types of violations has Eli Lilly & Co received?

Eli Lilly & Co has been cited for 2 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 & Co come from?

All FDA import refusal data for Eli Lilly & Co 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.