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Maria del Pilar de la Vega Villa

⚠️ Moderate Risk

FEI: 3010124263 • Queretaro, Queretaro • MEXICO

FEI

FEI Number

3010124263

📍

Location

Queretaro, Queretaro

🇲🇽

Country

MEXICO
🏢

Address

Boulevard Centro sur 3101, Col. COLINAS DEL CIMATARIO, Queretaro, Queretaro, Mexico

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
1
Unique Violations
11/14/2012
Latest Refusal
11/14/2012
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

2411×

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

DateProductViolationsDivision
11/14/2012
20NGC05PRICKLE PEAR (CORE FRUIT)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Maria del Pilar de la Vega Villa's FDA import refusal history?

Maria del Pilar de la Vega Villa (FEI: 3010124263) has 1 FDA import refusal record(s) in our database, spanning from 11/14/2012 to 11/14/2012.

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 del Pilar de la Vega Villa's FEI number is 3010124263.

What types of violations has Maria del Pilar de la Vega Villa received?

Maria del Pilar de la Vega Villa 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 del Pilar de la Vega Villa come from?

All FDA import refusal data for Maria del Pilar de la Vega Villa 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.