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SHIMANTO UNAGI

⚠️ Moderate Risk

FEI: 3013924334 • Takaoka-Gun, Kochi • JAPAN

FEI

FEI Number

3013924334

📍

Location

Takaoka-Gun, Kochi

🇯🇵

Country

JAPAN
🏢

Address

896-6, Mitsuke; Shimanto-Cho, Takaoka-Gun, Kochi, Japan

Moderate Risk

FDA Import Risk Assessment

37.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
6/21/2019
Latest Refusal
6/21/2019
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

2493×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

4733×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
6/21/2019
16CGY15EELS, CAKES, BALLS, ETC.
249FILTHY
473LABELING
Division of Southeast Imports (DSEI)
6/21/2019
16CGY15EELS, CAKES, BALLS, ETC.
249FILTHY
473LABELING
Division of Southeast Imports (DSEI)
6/21/2019
16CGY15EELS, CAKES, BALLS, ETC.
249FILTHY
473LABELING
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SHIMANTO UNAGI's FDA import refusal history?

SHIMANTO UNAGI (FEI: 3013924334) has 3 FDA import refusal record(s) in our database, spanning from 6/21/2019 to 6/21/2019.

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. SHIMANTO UNAGI's FEI number is 3013924334.

What types of violations has SHIMANTO UNAGI received?

SHIMANTO UNAGI has been cited for 2 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 SHIMANTO UNAGI come from?

All FDA import refusal data for SHIMANTO UNAGI 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.