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Leica Fiskeprodukter

⚠️ Moderate Risk

FEI: 13652 • Leirvikham, Norddyroy • NORWAY

FEI

FEI Number

13652

📍

Location

Leirvikham, Norddyroy

🇳🇴

Country

NORWAY
🏢

Address

O Meland, Box 7273, Leirvikham, Norddyroy, Norway

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/4/2003
Latest Refusal
2/4/2003
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2951×

LISTERIA

The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.

Refusal History

DateProductViolationsDivision
2/4/2003
16SVT32SALMON (HUMPBACK, SILVER, KING, SOCKEYE, ETC.), COLD SMOKED, FISH
295LISTERIA
New York District Office (NYK-DO)

Frequently Asked Questions

What is Leica Fiskeprodukter's FDA import refusal history?

Leica Fiskeprodukter (FEI: 13652) has 1 FDA import refusal record(s) in our database, spanning from 2/4/2003 to 2/4/2003.

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. Leica Fiskeprodukter's FEI number is 13652.

What types of violations has Leica Fiskeprodukter received?

Leica Fiskeprodukter 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 Leica Fiskeprodukter come from?

All FDA import refusal data for Leica Fiskeprodukter 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.