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MIYOSHI SHOKUHIN CO.,LTD.

⚠️ Moderate Risk

FEI: 3006754623 • Miyoshi, Tokushima • JAPAN

FEI

FEI Number

3006754623

📍

Location

Miyoshi, Tokushima

🇯🇵

Country

JAPAN
🏢

Address

604-1, Minochoshimizu, Miyoshi, Tokushima, 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
6/28/2011
Latest Refusal
6/28/2011
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
6/28/2011
16AGH73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
308MFR INSAN
Los Angeles District Office (LOS-DO)
6/28/2011
16AGH73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22')
308MFR INSAN
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is MIYOSHI SHOKUHIN CO.,LTD.'s FDA import refusal history?

MIYOSHI SHOKUHIN CO.,LTD. (FEI: 3006754623) has 2 FDA import refusal record(s) in our database, spanning from 6/28/2011 to 6/28/2011.

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. MIYOSHI SHOKUHIN CO.,LTD.'s FEI number is 3006754623.

What types of violations has MIYOSHI SHOKUHIN CO.,LTD. received?

MIYOSHI SHOKUHIN CO.,LTD. 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 MIYOSHI SHOKUHIN CO.,LTD. come from?

All FDA import refusal data for MIYOSHI SHOKUHIN 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.