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EURL KISKRANE

⚠️ Moderate Risk

FEI: 3013473823 • Biskra Ctr, Biskra • ALGERIA

FEI

FEI Number

3013473823

📍

Location

Biskra Ctr, Biskra

🇩🇿

Country

ALGERIA
🏢

Address

Km 3 Route de Taouggour, , Biskra Ctr, Biskra, Algeria

Moderate Risk

FDA Import Risk Assessment

49.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
2/13/2018
Latest Refusal
2/13/2018
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
2/13/2018
21GFT05DATES (PIT FRUIT), (PIT FRUIT)
249FILTHY
Division of Northern Border Imports (DNBI)
2/13/2018
21GFT05DATES (PIT FRUIT), (PIT FRUIT)
249FILTHY
Division of Northern Border Imports (DNBI)
2/13/2018
21GFT05DATES (PIT FRUIT), (PIT FRUIT)
249FILTHY
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is EURL KISKRANE's FDA import refusal history?

EURL KISKRANE (FEI: 3013473823) has 3 FDA import refusal record(s) in our database, spanning from 2/13/2018 to 2/13/2018.

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. EURL KISKRANE's FEI number is 3013473823.

What types of violations has EURL KISKRANE received?

EURL KISKRANE 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 EURL KISKRANE come from?

All FDA import refusal data for EURL KISKRANE 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.