Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai
⚠️ Moderate Risk
FEI: 3004471868 • Ushibuka • JAPAN
FEI Number
3004471868
Location
Ushibuka
Country
JAPANAddress
1550 33 Japan, Ushibuka; Machi, Ushibuka, , 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 |
|---|---|---|---|
| 10/28/2004 | 16AVT79YELLOWTAIL, AMBERJACK | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 9/20/2004 | 16AVT79YELLOWTAIL, AMBERJACK | 308MFR INSAN | Division of West Coast Imports (DWCI) |
| 1/22/2003 | 16AGT80BREAM | 308MFR INSAN | San Francisco District Office (SAN-DO) |
| 1/22/2003 | 16AGT79YELLOWTAIL, AMBERJACK | 308MFR INSAN | San Francisco District Office (SAN-DO) |
| 1/22/2003 | 16AGT79YELLOWTAIL, AMBERJACK | 308MFR INSAN | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai's FDA import refusal history?
Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai (FEI: 3004471868) has 5 FDA import refusal record(s) in our database, spanning from 1/22/2003 to 10/28/2004.
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. Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai's FEI number is 3004471868.
What types of violations has Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai received?
Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai 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 Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai come from?
All FDA import refusal data for Kumamoto-Ken Youshoku Gyogyou Kyoudo Kumiai 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.