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Grytestranda Fiskeindustri AS

⚠️ Moderate Risk

FEI: 3004342337 • Vatne, More og Romsdal • NORWAY

FEI

FEI Number

3004342337

📍

Location

Vatne, More og Romsdal

🇳🇴

Country

NORWAY
🏢

Address

Grytestranda, Vatne 6265, Vatne, More og Romsdal, Norway

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
8/16/2011
Latest Refusal
8/16/2011
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

25801×

MFRHACCP

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).

Refusal History

DateProductViolationsDivision
8/16/2011
16AGP12COD
2580MFRHACCP
New England District Office (NWE-DO)

Frequently Asked Questions

What is Grytestranda Fiskeindustri AS's FDA import refusal history?

Grytestranda Fiskeindustri AS (FEI: 3004342337) has 1 FDA import refusal record(s) in our database, spanning from 8/16/2011 to 8/16/2011.

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. Grytestranda Fiskeindustri AS's FEI number is 3004342337.

What types of violations has Grytestranda Fiskeindustri AS received?

Grytestranda Fiskeindustri AS 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 Grytestranda Fiskeindustri AS come from?

All FDA import refusal data for Grytestranda Fiskeindustri AS 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.