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OHORI CO.,LTD. IMAICHI FACTORY

⚠️ Moderate Risk

FEI: 3004248565 • Nikko, Tochigi • JAPAN

FEI

FEI Number

3004248565

📍

Location

Nikko, Tochigi

🇯🇵

Country

JAPAN
🏢

Address

2081-101, Shionomuro-Machi, Nikko, Tochigi, Japan

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
10/28/2015
Latest Refusal
9/24/2015
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

24202×

RADIONUC

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

Refusal History

DateProductViolationsDivision
10/28/2015
25SGT09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C.
2420RADIONUC
Division of Northeast Imports (DNEI)
9/24/2015
25SGT09FUNGUS, BLACK (CLOUD EARS), FUNGI PRODUCTS, N.E.C.
2420RADIONUC
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is OHORI CO.,LTD. IMAICHI FACTORY's FDA import refusal history?

OHORI CO.,LTD. IMAICHI FACTORY (FEI: 3004248565) has 2 FDA import refusal record(s) in our database, spanning from 9/24/2015 to 10/28/2015.

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. OHORI CO.,LTD. IMAICHI FACTORY's FEI number is 3004248565.

What types of violations has OHORI CO.,LTD. IMAICHI FACTORY received?

OHORI CO.,LTD. IMAICHI FACTORY 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 OHORI CO.,LTD. IMAICHI FACTORY come from?

All FDA import refusal data for OHORI CO.,LTD. IMAICHI FACTORY 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.