Marcas De Renombre Sa De Cv
✅ Low Risk
FEI: 3007369194 • Anzures • MEXICO
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/15/2009 | 53GY99OTHER MAKEUP PREPARATION, NOT FOR THE EYES, N.E.C. | 471CSTIC LBLG | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Marcas De Renombre Sa De Cv's FDA import refusal history?
Marcas De Renombre Sa De Cv (FEI: 3007369194) has 1 FDA import refusal record(s) in our database, spanning from 5/15/2009 to 5/15/2009.
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. Marcas De Renombre Sa De Cv's FEI number is 3007369194.
What types of violations has Marcas De Renombre Sa De Cv received?
Marcas De Renombre 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 Marcas De Renombre Sa De Cv come from?
All FDA import refusal data for Marcas De Renombre 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.