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Eli Lilly Nederland

⚠️ Moderate Risk

FEI: 3003726675 • Houten, Utrecht • NETHERLANDS

FEI

FEI Number

3003726675

📍

Location

Houten, Utrecht

🇳🇱
🏢

Address

Grootslag 1-5, , Houten, Utrecht, Netherlands

Moderate Risk

FDA Import Risk Assessment

44.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

4
Total Refusals
1
Unique Violations
2/16/2018
Latest Refusal
10/17/2003
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
2.8×10%
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

754×

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
2/16/2018
61PCY17INSULIN (INJ) (ANTI-DIABETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/14/2015
66SCA51TADALAFIL
75UNAPPROVED
New Orleans District Office (NOL-DO)
5/23/2012
65PDB03TAMSULOSIN HCL (REGULATOR)
75UNAPPROVED
New Orleans District Office (NOL-DO)
10/17/2003
65PDB02SILDENAFIL CITRATE (REGULATOR)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Eli Lilly Nederland's FDA import refusal history?

Eli Lilly Nederland (FEI: 3003726675) has 4 FDA import refusal record(s) in our database, spanning from 10/17/2003 to 2/16/2018.

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 Nederland's FEI number is 3003726675.

What types of violations has Eli Lilly Nederland received?

Eli Lilly Nederland 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 Nederland come from?

All FDA import refusal data for Eli Lilly Nederland 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.