ImportRefusal LogoImportRefusal

KANEICHI KOYANAGI SYOTEN

⚠️ Moderate Risk

FEI: 3012762674 • Shizuoka, Shizuoka • JAPAN

FEI

FEI Number

3012762674

📍

Location

Shizuoka, Shizuoka

🇯🇵

Country

JAPAN
🏢

Address

Sekibe; Suruga; 14-4; Sekibe; Suruga, Suruga; Sekibe; Suruga, Shizuoka, Shizuoka, Japan

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
8/26/2014
Latest Refusal
8/26/2014
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
8/26/2014
16AGN33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
308MFR INSAN
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is KANEICHI KOYANAGI SYOTEN's FDA import refusal history?

KANEICHI KOYANAGI SYOTEN (FEI: 3012762674) has 1 FDA import refusal record(s) in our database, spanning from 8/26/2014 to 8/26/2014.

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. KANEICHI KOYANAGI SYOTEN's FEI number is 3012762674.

What types of violations has KANEICHI KOYANAGI SYOTEN received?

KANEICHI KOYANAGI SYOTEN 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 KANEICHI KOYANAGI SYOTEN come from?

All FDA import refusal data for KANEICHI KOYANAGI SYOTEN 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.