Eli Lilly & Company
⚠️ Moderate Risk
FEI: 3006505136 • Stamford, CT • UNITED STATES
FEI Number
3006505136
Location
Stamford, CT
Country
UNITED STATESAddress
9 W Broad St Ste 6, , Stamford, CT, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/20/2001 | 61PCK54LISPRO INSULIN (ANTI-DIABETIC) | 342PERSONALRX | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Eli Lilly & Company's FDA import refusal history?
Eli Lilly & Company (FEI: 3006505136) has 1 FDA import refusal record(s) in our database, spanning from 12/20/2001 to 12/20/2001.
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 & Company's FEI number is 3006505136.
What types of violations has Eli Lilly & Company received?
Eli Lilly & 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 & Company come from?
All FDA import refusal data for Eli Lilly & 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.