Simatelex Manufactory Company Limited
⚠️ Moderate Risk
FEI: 1000228946 • Chaiwan • 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
INSANITARY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/4/2010 | 52AOA51COFFEE MAKER (PERCOLATOR, DRIP, ESPRESSO, CAPPUCCINO) (FOODWARE, COOKWARE & TABLEWARE) | 306INSANITARY | New York District Office (NYK-DO) |
| 3/4/2010 | 52AOA51COFFEE MAKER (PERCOLATOR, DRIP, ESPRESSO, CAPPUCCINO) (FOODWARE, COOKWARE & TABLEWARE) | 306INSANITARY | New York District Office (NYK-DO) |
| 3/4/2010 | 52AOA51COFFEE MAKER (PERCOLATOR, DRIP, ESPRESSO, CAPPUCCINO) (FOODWARE, COOKWARE & TABLEWARE) | 306INSANITARY | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Simatelex Manufactory Company Limited's FDA import refusal history?
Simatelex Manufactory Company Limited (FEI: 1000228946) has 3 FDA import refusal record(s) in our database, spanning from 3/4/2010 to 3/4/2010.
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. Simatelex Manufactory Company Limited's FEI number is 1000228946.
What types of violations has Simatelex Manufactory Company Limited received?
Simatelex Manufactory Company Limited 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 Simatelex Manufactory Company Limited come from?
All FDA import refusal data for Simatelex Manufactory Company Limited 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.