Yamaji Co Ltd
⚠️ Moderate Risk
FEI: 3005131432 • Saiki, Oita • 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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/13/2014 | 16AGT33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 308MFR INSAN | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Yamaji Co Ltd's FDA import refusal history?
Yamaji Co Ltd (FEI: 3005131432) has 1 FDA import refusal record(s) in our database, spanning from 1/13/2014 to 1/13/2014.
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. Yamaji Co Ltd's FEI number is 3005131432.
What types of violations has Yamaji Co Ltd received?
Yamaji 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 Yamaji Co Ltd come from?
All FDA import refusal data for Yamaji 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.