EXPORTADORA 6 DE ENERO
⚠️ High Risk
FEI: 3005357585 • San Nicolas De Los Garza, Nuevo Leon • MEXICO
FEI Number
3005357585
Location
San Nicolas De Los Garza, Nuevo Leon
Country
MEXICOAddress
Ave Los Angeles # 1000, , San Nicolas De Los Garza, Nuevo Leon, 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 |
|---|---|---|---|
| 1/30/2006 | 24HFH08PEPPER, HOT, DRIED OR PASTE | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 1/19/2006 | 24HFH08PEPPER, HOT, DRIED OR PASTE | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 11/17/2005 | 24FFH08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 249FILTHY | Division of Southwest Imports (DSWI) |
| 11/17/2005 | 24FFH08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 249FILTHY | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is EXPORTADORA 6 DE ENERO's FDA import refusal history?
EXPORTADORA 6 DE ENERO (FEI: 3005357585) has 4 FDA import refusal record(s) in our database, spanning from 11/17/2005 to 1/30/2006.
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 6 DE ENERO's FEI number is 3005357585.
What types of violations has EXPORTADORA 6 DE ENERO received?
EXPORTADORA 6 DE ENERO 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 6 DE ENERO come from?
All FDA import refusal data for EXPORTADORA 6 DE ENERO 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.