Hachinohe Toyo Co Ltd
✅ Low Risk
FEI: 1000358836 • Hachinohe, Aomori Pref • JAPAN
FEI Number
1000358836
Location
Hachinohe, Aomori Pref
Country
JAPANAddress
2 629 Aza,, Ooazachoshichiyachi, Hachinohe, Aomori Pref, Japan
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/9/2002 | 04CHT08ORIENTAL NOODLES (FLAVORED WITH SHRIMP,CHICKEN,BEEF,LOBSTER,CRAB,PLAIN,ETC.) | 218LIST INGRE | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Hachinohe Toyo Co Ltd's FDA import refusal history?
Hachinohe Toyo Co Ltd (FEI: 1000358836) has 1 FDA import refusal record(s) in our database, spanning from 8/9/2002 to 8/9/2002.
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. Hachinohe Toyo Co Ltd's FEI number is 1000358836.
What types of violations has Hachinohe Toyo Co Ltd received?
Hachinohe Toyo 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 Hachinohe Toyo Co Ltd come from?
All FDA import refusal data for Hachinohe Toyo 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.