Ana Maria Avila Lopez
⚠️ Moderate Risk
FEI: 3003592420 • Montemorelos, Nuevo Leon • MEXICO
FEI Number
3003592420
Location
Montemorelos, Nuevo Leon
Country
MEXICOAddress
Principal S/N, Col. San Miguel, Montemorelos, Nuevo Leon, Mexico
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/21/2003 | 24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 9/12/2002 | 20NFC05PRICKLE PEAR (CORE FRUIT) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 9/6/2002 | 24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Ana Maria Avila Lopez's FDA import refusal history?
Ana Maria Avila Lopez (FEI: 3003592420) has 3 FDA import refusal record(s) in our database, spanning from 9/6/2002 to 7/21/2003.
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. Ana Maria Avila Lopez's FEI number is 3003592420.
What types of violations has Ana Maria Avila Lopez received?
Ana Maria Avila 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 Ana Maria Avila Lopez come from?
All FDA import refusal data for Ana Maria Avila 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.