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Okashinomori Middle Spoon

⚠️ Moderate Risk

FEI: 3010157187 • Nishio, Aichi • JAPAN

FEI

FEI Number

3010157187

📍

Location

Nishio, Aichi

🇯🇵

Country

JAPAN
🏢

Address

7-9, Yonezu-Cho, Nishio, Aichi, Japan

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
8/15/2013
Latest Refusal
8/15/2013
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

Refusal History

DateProductViolationsDivision
8/15/2013
20RGT01APPLE, JAM, JELLY, PRESERVES, MARMALADE, BUTTER AND CANDIED
11UNSAFE COL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Okashinomori Middle Spoon's FDA import refusal history?

Okashinomori Middle Spoon (FEI: 3010157187) has 1 FDA import refusal record(s) in our database, spanning from 8/15/2013 to 8/15/2013.

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. Okashinomori Middle Spoon's FEI number is 3010157187.

What types of violations has Okashinomori Middle Spoon received?

Okashinomori Middle Spoon 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 Okashinomori Middle Spoon come from?

All FDA import refusal data for Okashinomori Middle Spoon 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.