Onimaru Co Ltd
⚠️ Moderate Risk
FEI: 3009208819 • Miyama, Fukuoka • JAPAN
FEI Number
3009208819
Location
Miyama, Fukuoka
Country
JAPANAddress
Ayahiro 1613-1, Setakamachioe, Miyama, Fukuoka, Japan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/10/2017 | 25JGT07RADISH (ROOT & TUBER VEGETABLE) | 11UNSAFE COL | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Onimaru Co Ltd's FDA import refusal history?
Onimaru Co Ltd (FEI: 3009208819) has 1 FDA import refusal record(s) in our database, spanning from 8/10/2017 to 8/10/2017.
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. Onimaru Co Ltd's FEI number is 3009208819.
What types of violations has Onimaru Co Ltd received?
Onimaru 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 Onimaru Co Ltd come from?
All FDA import refusal data for Onimaru 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.