Koichi Kizaki
⚠️ High Risk
FEI: 3002929408 • Tamana, Kumamoto • JAPAN
FEI Number
3002929408
Location
Tamana, Kumamoto
Country
JAPANAddress
721 3, Hakoya, Tamana, Kumamoto, Japan
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/4/2001 | 16MGD09OCTOPUS, OTHER AQUATIC SPECIES | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT22MACKEREL (ONLY SCOMBEROMORUS SPP EG. SPANISH OR KING) | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT73MACKEREL (ALL EXCEPT SCOMBEROMORUS SP, EG SPANISH OR KING SEE '22') | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT80BREAM | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT15EEL | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT56FILEFISH | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT07BONITO | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT79YELLOWTAIL, AMBERJACK | 249FILTHY | Los Angeles District Office (LOS-DO) |
| 10/4/2001 | 16AGT79YELLOWTAIL, AMBERJACK | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Koichi Kizaki's FDA import refusal history?
Koichi Kizaki (FEI: 3002929408) has 9 FDA import refusal record(s) in our database, spanning from 10/4/2001 to 10/4/2001.
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. Koichi Kizaki's FEI number is 3002929408.
What types of violations has Koichi Kizaki received?
Koichi Kizaki 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 Koichi Kizaki come from?
All FDA import refusal data for Koichi Kizaki 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.