MARIA IVETTE LUNA ESCOBAR
⚠️ High Risk
FEI: 3040035648 • Tulcingo De Valle • MEXICO
FEI Number
3040035648
Location
Tulcingo De Valle
Country
MEXICOAddress
Benito Juarez N 105, Puebla, Tulcingo De Valle, , 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
Frequently Asked Questions
What is MARIA IVETTE LUNA ESCOBAR's FDA import refusal history?
MARIA IVETTE LUNA ESCOBAR (FEI: 3040035648) has 3 FDA import refusal record(s) in our database, spanning from 10/27/2025 to 12/1/2025.
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. MARIA IVETTE LUNA ESCOBAR's FEI number is 3040035648.
What types of violations has MARIA IVETTE LUNA ESCOBAR received?
MARIA IVETTE LUNA ESCOBAR 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 IVETTE LUNA ESCOBAR come from?
All FDA import refusal data for MARIA IVETTE LUNA ESCOBAR 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.