MARIA GUADALUPE NAVARRO LOPEZ
⚠️ High Risk
FEI: 3015423078 • Aguascalientes, Aguascalientes • MEXICO
FEI Number
3015423078
Location
Aguascalientes, Aguascalientes
Country
MEXICOAddress
Calle El Redondel Trojes De Orient 139, Fracc. Villa De Las Trojes, Aguascalientes, Aguascalientes, Aguascalientes, 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 |
|---|---|---|---|
| 8/26/2021 | 21TFB14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Southwest Imports (DSWI) |
| 7/23/2021 | 21TFH14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Southwest Imports (DSWI) |
| 3/11/2021 | 21TFH14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Southwest Imports (DSWI) |
| 7/20/2020 | 21TFB14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is MARIA GUADALUPE NAVARRO LOPEZ's FDA import refusal history?
MARIA GUADALUPE NAVARRO LOPEZ (FEI: 3015423078) has 4 FDA import refusal record(s) in our database, spanning from 7/20/2020 to 8/26/2021.
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. MARIA GUADALUPE NAVARRO LOPEZ's FEI number is 3015423078.
What types of violations has MARIA GUADALUPE NAVARRO LOPEZ received?
MARIA GUADALUPE NAVARRO LOPEZ 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 MARIA GUADALUPE NAVARRO LOPEZ come from?
All FDA import refusal data for MARIA GUADALUPE NAVARRO LOPEZ 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.