SANOFI AVENTIS DE MEXICO SA CV
⚠️ High Risk
FEI: 3032091024 • Mexico City • MEXICO
FEI Number
3032091024
Location
Mexico City
Country
MEXICOAddress
Alto Lerma Aqueduct No, , Mexico City, , 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/29/2025 | 61PDB37INSULIN PURIFIED HUMAN SEMISYNTHETIC (ANTI-DIABETIC) | Division of Southeast Imports (DSEI) | |
| 5/28/2025 | 60LCA21DIPYRONE (ANALGESIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 5/13/2025 | 60LDB99ANALGESIC, N.E.C. | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SANOFI AVENTIS DE MEXICO SA CV's FDA import refusal history?
SANOFI AVENTIS DE MEXICO SA CV (FEI: 3032091024) has 3 FDA import refusal record(s) in our database, spanning from 5/13/2025 to 10/29/2025.
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. SANOFI AVENTIS DE MEXICO SA CV's FEI number is 3032091024.
What types of violations has SANOFI AVENTIS DE MEXICO SA CV received?
SANOFI AVENTIS DE MEXICO SA CV has been cited for 2 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 SANOFI AVENTIS DE MEXICO SA CV come from?
All FDA import refusal data for SANOFI AVENTIS DE MEXICO SA 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.