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SANUKI KANZUME CO., MINO PLANT

⚠️ Moderate Risk

FEI: 3003244067 • Mitoyo, Kagawa • JAPAN

FEI

FEI Number

3003244067

📍

Location

Mitoyo, Kagawa

🇯🇵

Country

JAPAN
🏢

Address

Omiko 3882, Minochoomi, Mitoyo, Kagawa, Japan

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
10/28/2008
Latest Refusal
10/28/2008
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

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
10/28/2008
24AEE16BLACK BEANS
83NO PROCESS
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is SANUKI KANZUME CO., MINO PLANT's FDA import refusal history?

SANUKI KANZUME CO., MINO PLANT (FEI: 3003244067) has 1 FDA import refusal record(s) in our database, spanning from 10/28/2008 to 10/28/2008.

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. SANUKI KANZUME CO., MINO PLANT's FEI number is 3003244067.

What types of violations has SANUKI KANZUME CO., MINO PLANT received?

SANUKI KANZUME CO., MINO PLANT 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 SANUKI KANZUME CO., MINO PLANT come from?

All FDA import refusal data for SANUKI KANZUME CO., MINO PLANT 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.