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Kaneka Eurogentec SA

⚠️ Moderate Risk

FEI: 3003323169 • Seraing, Liege • BELGIUM

FEI

FEI Number

3003323169

📍

Location

Seraing, Liege

🇧🇪

Country

BELGIUM
🏢

Address

Rue Du Bois St-Jean 14, , Seraing, Liege, Belgium

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/23/2020
Latest Refusal
11/23/2020
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

22801×

DIRSEXMPT

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.

Refusal History

DateProductViolationsDivision
11/23/2020
66WIK99IMMUNOMODULATOR N.E.C.
2280DIRSEXMPT
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Kaneka Eurogentec SA's FDA import refusal history?

Kaneka Eurogentec SA (FEI: 3003323169) has 1 FDA import refusal record(s) in our database, spanning from 11/23/2020 to 11/23/2020.

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. Kaneka Eurogentec SA's FEI number is 3003323169.

What types of violations has Kaneka Eurogentec SA received?

Kaneka Eurogentec SA 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 Kaneka Eurogentec SA come from?

All FDA import refusal data for Kaneka Eurogentec SA 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.