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KANEKO SANGYO CO., LTD SECOND FACTORY

⚠️ Moderate Risk

FEI: 3011137880 • Karatsu, Saga • JAPAN

FEI

FEI Number

3011137880

📍

Location

Karatsu, Saga

🇯🇵

Country

JAPAN
🏢

Address

1-8, Nakanosedori, Karatsu, Saga, Japan

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
7/6/2006
Latest Refusal
7/6/2006
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

20002×

IMPTRHACCP

The food appears to have been prepared, packed or held under insanitary conditions, or may have become injurious to health, due to the failure of the importer to provide verification of compliance pursuant to 21 CFR 123.12(d).

Refusal History

DateProductViolationsDivision
7/6/2006
16AGT79YELLOWTAIL, AMBERJACK
2000IMPTRHACCP
Los Angeles District Office (LOS-DO)
7/6/2006
16AGT79YELLOWTAIL, AMBERJACK
2000IMPTRHACCP
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is KANEKO SANGYO CO., LTD SECOND FACTORY's FDA import refusal history?

KANEKO SANGYO CO., LTD SECOND FACTORY (FEI: 3011137880) has 2 FDA import refusal record(s) in our database, spanning from 7/6/2006 to 7/6/2006.

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. KANEKO SANGYO CO., LTD SECOND FACTORY's FEI number is 3011137880.

What types of violations has KANEKO SANGYO CO., LTD SECOND FACTORY received?

KANEKO SANGYO CO., LTD SECOND FACTORY 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 KANEKO SANGYO CO., LTD SECOND FACTORY come from?

All FDA import refusal data for KANEKO SANGYO CO., LTD SECOND FACTORY 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.