Unllever De Mexico Sa De Cv
⚠️ High Risk
FEI: 3003459263 • Tultitlan Edo Mexico • MEXICO
FEI Number
3003459263
Location
Tultitlan Edo Mexico
Country
MEXICOAddress
Av Repalca No 2, Col Rancho Stodomingo, Tultitlan Edo Mexico, , Mexico
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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 |
|---|---|---|---|
| 8/31/2023 | 53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | 197COSM COLOR | Division of Southwest Imports (DSWI) |
| 8/31/2023 | 53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | 197COSM COLOR | Division of Southwest Imports (DSWI) |
| 8/31/2023 | 53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | 197COSM COLOR | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Unllever De Mexico Sa De Cv's FDA import refusal history?
Unllever De Mexico Sa De Cv (FEI: 3003459263) has 3 FDA import refusal record(s) in our database, spanning from 8/31/2023 to 8/31/2023.
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. Unllever De Mexico Sa De Cv's FEI number is 3003459263.
What types of violations has Unllever De Mexico Sa De Cv received?
Unllever De Mexico Sa De Cv 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 Unllever De Mexico Sa De Cv come from?
All FDA import refusal data for Unllever De Mexico Sa De Cv 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.