Surefil Beauty Products
⚠️ Moderate Risk
FEI: 3004725666 • St. Helens, Merseyside • UNITED KINGDOM
FEI Number
3004725666
Location
St. Helens, Merseyside
Country
UNITED KINGDOMAddress
The Bedford Centre Unit 10, Bedford Street, St. Helens, Merseyside, United Kingdom
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
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/19/2015 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Los Angeles District Office (LOS-DO) |
| 6/29/2011 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Seattle District Office (SEA-DO) |
| 6/29/2011 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Seattle District Office (SEA-DO) |
| 6/29/2011 | 53CH03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Surefil Beauty Products's FDA import refusal history?
Surefil Beauty Products (FEI: 3004725666) has 4 FDA import refusal record(s) in our database, spanning from 6/29/2011 to 10/19/2015.
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. Surefil Beauty Products's FEI number is 3004725666.
What types of violations has Surefil Beauty Products received?
Surefil Beauty Products 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 Surefil Beauty Products come from?
All FDA import refusal data for Surefil Beauty Products 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.