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Kaneman Murase Co Ltd

⚠️ Moderate Risk

FEI: 1000116830 • Osaka, Osaka • JAPAN

FEI

FEI Number

1000116830

📍

Location

Osaka, Osaka

🇯🇵

Country

JAPAN
🏢

Address

1 Chome 15-16, Utsubohon-Machi; Nishi, Osaka, Osaka, Japan

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
12/31/2002
Latest Refusal
12/31/2002
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
12/31/2002
25JGP04SCALLIONS, GREEN ONIONS (ROOT & TUBER VEGETABLE)
260FALSE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Kaneman Murase Co Ltd's FDA import refusal history?

Kaneman Murase Co Ltd (FEI: 1000116830) has 1 FDA import refusal record(s) in our database, spanning from 12/31/2002 to 12/31/2002.

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. Kaneman Murase Co Ltd's FEI number is 1000116830.

What types of violations has Kaneman Murase Co Ltd received?

Kaneman Murase Co Ltd has been cited for 2 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 Kaneman Murase Co Ltd come from?

All FDA import refusal data for Kaneman Murase 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.