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MARUDAI MINAMI SHOKUHIN

⚠️ Moderate Risk

FEI: 3012906656 • Hakodate, Hokkai-do • JAPAN

FEI

FEI Number

3012906656

📍

Location

Hakodate, Hokkai-do

🇯🇵

Country

JAPAN
🏢

Address

139-30, Akagawa-Cho, Hakodate, Hokkai-do, 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
3/11/2020
Latest Refusal
3/11/2020
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

25802×

MFRHACCP

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).

Refusal History

DateProductViolationsDivision
3/11/2020
16AGT21HERRING
2580MFRHACCP
Division of West Coast Imports (DWCI)
3/11/2020
16MGT03SQUID, OTHER AQUATIC SPECIES
2580MFRHACCP
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is MARUDAI MINAMI SHOKUHIN's FDA import refusal history?

MARUDAI MINAMI SHOKUHIN (FEI: 3012906656) has 2 FDA import refusal record(s) in our database, spanning from 3/11/2020 to 3/11/2020.

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. MARUDAI MINAMI SHOKUHIN's FEI number is 3012906656.

What types of violations has MARUDAI MINAMI SHOKUHIN received?

MARUDAI MINAMI SHOKUHIN 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 MARUDAI MINAMI SHOKUHIN come from?

All FDA import refusal data for MARUDAI MINAMI SHOKUHIN 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.