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Mizunaga Suisan

⚠️ Moderate Risk

FEI: 3004321617 • Higashiusuki-Gun, Miyazaki • JAPAN

FEI

FEI Number

3004321617

📍

Location

Higashiusuki-Gun, Miyazaki

🇯🇵

Country

JAPAN
🏢

Address

9083-1 Higashi Usuki Gun, Oazakadogawaozue; Kadogawa-Cho, Higashiusuki-Gun, Miyazaki, Japan

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
9/25/2013
Latest Refusal
9/25/2013
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

3082×

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
9/25/2013
16AGN33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
308MFR INSAN
Los Angeles District Office (LOS-DO)
9/25/2013
16AGN33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.)
308MFR INSAN
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Mizunaga Suisan's FDA import refusal history?

Mizunaga Suisan (FEI: 3004321617) has 2 FDA import refusal record(s) in our database, spanning from 9/25/2013 to 9/25/2013.

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. Mizunaga Suisan's FEI number is 3004321617.

What types of violations has Mizunaga Suisan received?

Mizunaga Suisan 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 Mizunaga Suisan come from?

All FDA import refusal data for Mizunaga Suisan 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.