HUNAN EKA CERAMICS
⚠️ Moderate Risk
FEI: 3013182705 • HUNAN • 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
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/23/2017 | 52AIE26CUPS, MUGS (FOODWARE, COOKWARE & TABLEWARE) | 251POISONOUS | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is HUNAN EKA CERAMICS's FDA import refusal history?
HUNAN EKA CERAMICS (FEI: 3013182705) has 1 FDA import refusal record(s) in our database, spanning from 8/23/2017 to 8/23/2017.
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. HUNAN EKA CERAMICS's FEI number is 3013182705.
What types of violations has HUNAN EKA CERAMICS received?
HUNAN EKA CERAMICS 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 HUNAN EKA CERAMICS come from?
All FDA import refusal data for HUNAN EKA CERAMICS 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.