Prosogo Cosmetics & Gifts Co Limited
⚠️ Moderate Risk
FEI: 3005000958 • Guangzhou, Guangdong • CHINA
FEI Number
3005000958
Location
Guangzhou, Guangdong
Country
CHINAAddress
2nd Floor, Bldg a Dachuang Industrial, Guangzhou, Guangdong, 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
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
Refusal History
Frequently Asked Questions
What is Prosogo Cosmetics & Gifts Co Limited's FDA import refusal history?
Prosogo Cosmetics & Gifts Co Limited (FEI: 3005000958) has 2 FDA import refusal record(s) in our database, spanning from 5/2/2005 to 5/2/2005.
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. Prosogo Cosmetics & Gifts Co Limited's FEI number is 3005000958.
What types of violations has Prosogo Cosmetics & Gifts Co Limited received?
Prosogo Cosmetics & Gifts Co 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 Prosogo Cosmetics & Gifts Co Limited come from?
All FDA import refusal data for Prosogo Cosmetics & Gifts Co 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.