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Vikenco

⚠️ Moderate Risk

FEI: 3009948417 • Aukra, NO-NOTA • NORWAY

FEI

FEI Number

3009948417

📍

Location

Aukra, NO-NOTA

🇳🇴

Country

NORWAY
🏢

Address

Rindaroyvegen 383, , Aukra, NO-NOTA, Norway

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
8/16/2006
Latest Refusal
8/8/2006
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

23603×

HISTAMINE

The article appears to bear or contain histamine, a poisonous and deleterious substance in such quantity as ordinarily renders it injurious to health.

Refusal History

DateProductViolationsDivision
8/16/2006
16XGD03SALMON, ALL, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2360HISTAMINE
Southwest Import District Office (SWI-DO)
8/16/2006
16XHC03SALMON, ALL, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2360HISTAMINE
Southwest Import District Office (SWI-DO)
8/8/2006
16XHC03SALMON, ALL, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2360HISTAMINE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Vikenco's FDA import refusal history?

Vikenco (FEI: 3009948417) has 3 FDA import refusal record(s) in our database, spanning from 8/8/2006 to 8/16/2006.

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. Vikenco's FEI number is 3009948417.

What types of violations has Vikenco received?

Vikenco 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 Vikenco come from?

All FDA import refusal data for Vikenco 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.