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Lilly Pharmaeutical

⚠️ Moderate Risk

FEI: 3003571949 • Giesen, Hesse • GERMANY

FEI

FEI Number

3003571949

📍

Location

Giesen, Hesse

🇩🇪

Country

GERMANY
🏢

Address

Teichweg 3, , Giesen, Hesse, Germany

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
2/12/2002
Latest Refusal
2/12/2002
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

3423×

PERSONALRX

The article appears to be a drug which requires a prescription from your doctor.

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
2/12/2002
66MCB03ALPRAZOLAM (TRANQUILIZER)
342PERSONALRX
75UNAPPROVED
Detroit District Office (DET-DO)
2/12/2002
66MCB03ALPRAZOLAM (TRANQUILIZER)
342PERSONALRX
75UNAPPROVED
Detroit District Office (DET-DO)
2/12/2002
66MCB03ALPRAZOLAM (TRANQUILIZER)
342PERSONALRX
75UNAPPROVED
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Lilly Pharmaeutical's FDA import refusal history?

Lilly Pharmaeutical (FEI: 3003571949) has 3 FDA import refusal record(s) in our database, spanning from 2/12/2002 to 2/12/2002.

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. Lilly Pharmaeutical's FEI number is 3003571949.

What types of violations has Lilly Pharmaeutical received?

Lilly Pharmaeutical 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 Lilly Pharmaeutical come from?

All FDA import refusal data for Lilly Pharmaeutical 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.