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AKITA SHOKUSAN, CO., LTD

⚠️ Moderate Risk

FEI: 3030149628 • Semboku-Gun Misato-Ch • JAPAN

FEI

FEI Number

3030149628

📍

Location

Semboku-Gun Misato-Ch

🇯🇵

Country

JAPAN
🏢

Address

205-1 Uwanootsu Tsuchizaki Semboku-Gun Misato-Cho, , Semboku-Gun Misato-Ch, , Japan

Moderate Risk

FDA Import Risk Assessment

49.1
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
9/11/2025
Latest Refusal
8/5/2025
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
17.7×30%
Recency
78.9×20%
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

112×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2742×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

Refusal History

DateProductViolationsDivision
9/11/2025
25JGP07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
Division of Northeast Imports (DNEI)
8/5/2025
25JGT07RADISH (ROOT & TUBER VEGETABLE)
11UNSAFE COL
274COLOR LBLG
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is AKITA SHOKUSAN, CO., LTD's FDA import refusal history?

AKITA SHOKUSAN, CO., LTD (FEI: 3030149628) has 2 FDA import refusal record(s) in our database, spanning from 8/5/2025 to 9/11/2025.

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. AKITA SHOKUSAN, CO., LTD's FEI number is 3030149628.

What types of violations has AKITA SHOKUSAN, CO., LTD received?

AKITA SHOKUSAN, CO., LTD 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 AKITA SHOKUSAN, CO., LTD come from?

All FDA import refusal data for AKITA SHOKUSAN, CO., LTD 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.