Exportadora La-Mex Sa De Cv
⚠️ High Risk
FEI: 3003324702 • Ver. • MEXICO
FEI Number
3003324702
Location
Ver.
Country
MEXICOAddress
Calle Rivera S/N Entre Rosa Y Clavel, , Pueblo Viejo, Ver., , 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/28/2003 | 16JHC01CRAB | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 11/7/2003 | 16JHC01CRAB | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 10/8/2003 | 16JHC01CRAB | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 8/7/2002 | 16JHC01CRAB | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 7/18/2002 | 16JHC01CRAB | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 5/30/2002 | 16JHC01CRAB | 249FILTHY | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Exportadora La-Mex Sa De Cv's FDA import refusal history?
Exportadora La-Mex Sa De Cv (FEI: 3003324702) has 6 FDA import refusal record(s) in our database, spanning from 5/30/2002 to 11/28/2003.
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. Exportadora La-Mex Sa De Cv's FEI number is 3003324702.
What types of violations has Exportadora La-Mex Sa De Cv received?
Exportadora La-Mex 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 Exportadora La-Mex Sa De Cv come from?
All FDA import refusal data for Exportadora La-Mex 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.