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AMGEN (EUROPE) GMBH

⚠️ High Risk

FEI: 3030486581 • Rotkreuz, Zug • SWITZERLAND

FEI

FEI Number

3030486581

📍

Location

Rotkreuz, Zug

🇨🇭
🏢

Address

Eori#Ch110612748, Suurstoffi 22, Rotkreuz, Zug, Switzerland

High Risk

FDA Import Risk Assessment

56.8
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/28/2025
Latest Refusal
2/28/2025
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
82.4×20%
Frequency
10.0×10%
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

751×

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
2/28/2025
58MDL10VEDOLIZUMAB
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AMGEN (EUROPE) GMBH's FDA import refusal history?

AMGEN (EUROPE) GMBH (FEI: 3030486581) has 1 FDA import refusal record(s) in our database, spanning from 2/28/2025 to 2/28/2025.

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. AMGEN (EUROPE) GMBH's FEI number is 3030486581.

What types of violations has AMGEN (EUROPE) GMBH received?

AMGEN (EUROPE) GMBH 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 AMGEN (EUROPE) GMBH come from?

All FDA import refusal data for AMGEN (EUROPE) GMBH 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.