Horyo Corporation
⚠️ Moderate Risk
FEI: 3012220555 • Narita, Chiba • JAPAN
FEI Number
3012220555
Location
Narita, Chiba
Country
JAPANAddress
2-45, Iinaka, Narita, Chiba, 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
RADIONUC
Article appears to contain the radionuclide, Cesium-137, a poisonous and deleterious substance which may render it injurious to health.
FORBIDDEN
The article is subject to refusal of admission pursuant to Section 801(a)(2) in that it appears to be forbidden or restricted in sale in the country in which it was produced or from which it was exported.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/31/2015 | 16AFC15EEL | Division of Northeast Imports (DNEI) | |
| 7/31/2015 | 16AFC15EEL | Division of Northeast Imports (DNEI) | |
| 6/1/2015 | 16AFC15EEL | Division of Northeast Imports (DNEI) | |
| 6/1/2015 | 16AFC15EEL | Division of Northeast Imports (DNEI) | |
| 5/29/2015 | 16AFC15EEL | 2420RADIONUC | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Horyo Corporation's FDA import refusal history?
Horyo Corporation (FEI: 3012220555) has 5 FDA import refusal record(s) in our database, spanning from 5/29/2015 to 7/31/2015.
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. Horyo Corporation's FEI number is 3012220555.
What types of violations has Horyo Corporation received?
Horyo Corporation has been cited for 2 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 Horyo Corporation come from?
All FDA import refusal data for Horyo Corporation 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.