China Rose Black Cosmetics
⚠️ Moderate Risk
FEI: 3009701840 • Guangrhou • CHINA
FEI Number
3009701840
Location
Guangrhou
Country
CHINAAddress
121 Guangyuan West Road, , Guangrhou, , 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
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
Frequently Asked Questions
What is China Rose Black Cosmetics's FDA import refusal history?
China Rose Black Cosmetics (FEI: 3009701840) has 2 FDA import refusal record(s) in our database, spanning from 10/3/2012 to 10/3/2012.
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. China Rose Black Cosmetics's FEI number is 3009701840.
What types of violations has China Rose Black Cosmetics received?
China Rose Black Cosmetics 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 China Rose Black Cosmetics come from?
All FDA import refusal data for China Rose Black Cosmetics 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.