Gloriental Ind Corp
⚠️ Moderate Risk
FEI: 3004466022 • Xiamen • CHINA
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
MELAMINE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to bear or contain a food additive, namely melamine and/or a melamine analog, that is unsafe within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/31/2009 | 34HET99CHOCOLATE AND COCOA BEVERAGE BASE, N.E.C. | 3421MELAMINE | Minneapolis District Office (MIN-DO) |
Frequently Asked Questions
What is Gloriental Ind Corp's FDA import refusal history?
Gloriental Ind Corp (FEI: 3004466022) has 1 FDA import refusal record(s) in our database, spanning from 3/31/2009 to 3/31/2009.
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. Gloriental Ind Corp's FEI number is 3004466022.
What types of violations has Gloriental Ind Corp received?
Gloriental Ind Corp 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 Gloriental Ind Corp come from?
All FDA import refusal data for Gloriental Ind Corp 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.