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OSHIMAEN CO.,LTD

⚠️ High Risk

FEI: 3007556803 • Edogawa, Tokyo • JAPAN

FEI

FEI Number

3007556803

📍

Location

Edogawa, Tokyo

🇯🇵

Country

JAPAN
🏢

Address

2 Chome 24-11, Matsue, Edogawa, Tokyo, Japan

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

4
Total Refusals
1
Unique Violations
6/7/2011
Latest Refusal
6/7/2011
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

24204×

RADIONUC

Article appears to contain the radionuclide, Cesium-137, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
6/7/2011
25SGT04MUSHROOM, SHIITAKE, FUNGI PRODUCTS, N.E.C.
2420RADIONUC
Los Angeles District Office (LOS-DO)
6/7/2011
25SGT04MUSHROOM, SHIITAKE, FUNGI PRODUCTS, N.E.C.
2420RADIONUC
Los Angeles District Office (LOS-DO)
6/7/2011
25SGT04MUSHROOM, SHIITAKE, FUNGI PRODUCTS, N.E.C.
2420RADIONUC
Los Angeles District Office (LOS-DO)
6/7/2011
25SGT04MUSHROOM, SHIITAKE, FUNGI PRODUCTS, N.E.C.
2420RADIONUC
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

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

OSHIMAEN CO.,LTD (FEI: 3007556803) has 4 FDA import refusal record(s) in our database, spanning from 6/7/2011 to 6/7/2011.

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. OSHIMAEN CO.,LTD's FEI number is 3007556803.

What types of violations has OSHIMAEN CO.,LTD received?

OSHIMAEN 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 OSHIMAEN CO.,LTD come from?

All FDA import refusal data for OSHIMAEN 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.