EISHINDO
⚠️ Moderate Risk
FEI: 3010124844 • Amagasaki, Hyogo • JAPAN
FEI Number
3010124844
Location
Amagasaki, Hyogo
Country
JAPANAddress
12-27, Meishin-Cho, Amagasaki, Hyogo, 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).
FOREIGN OB
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.
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 |
|---|---|---|---|
| 4/2/2021 | 33MGT01GEL CUPS, FRUIT FLAVORED | Division of Northeast Imports (DNEI) | |
| 3/31/2021 | 33MGT01GEL CUPS, FRUIT FLAVORED | Division of Northeast Imports (DNEI) | |
| 2/9/2021 | 33LGT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 157FOREIGN OB | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is EISHINDO's FDA import refusal history?
EISHINDO (FEI: 3010124844) has 3 FDA import refusal record(s) in our database, spanning from 2/9/2021 to 4/2/2021.
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. EISHINDO's FEI number is 3010124844.
What types of violations has EISHINDO received?
EISHINDO has been cited for 3 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 EISHINDO come from?
All FDA import refusal data for EISHINDO 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.