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Maria Hernandez

⚠️ Moderate Risk

FEI: 3004000903 • Iguala Gro • MEXICO

FEI

FEI Number

3004000903

📍

Location

Iguala Gro

🇲🇽

Country

MEXICO
🏢

Address

Calle Alarcon #60, , Iguala Gro, , Mexico

Moderate Risk

FDA Import Risk Assessment

45.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
6/30/2003
Latest Refusal
6/2/2003
Earliest Refusal

Score Breakdown

Violation Severity
95.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2811×

BACTERIA

The article appears to contain a poisonous and deleterious substance which may render it injurious to health. Contains

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
6/30/2003
12CGH13CHEESE, HISPANIC/LATINO/MEXICAN STYLE, ALL VARIETIES, INCLUDING QUESO
281BACTERIA
Chicago District Office (CHI-DO)
6/2/2003
12CGH13CHEESE, HISPANIC/LATINO/MEXICAN STYLE, ALL VARIETIES, INCLUDING QUESO
308MFR INSAN
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Maria Hernandez's FDA import refusal history?

Maria Hernandez (FEI: 3004000903) has 2 FDA import refusal record(s) in our database, spanning from 6/2/2003 to 6/30/2003.

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. Maria Hernandez's FEI number is 3004000903.

What types of violations has Maria Hernandez received?

Maria Hernandez has been cited for 2 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 Hernandez come from?

All FDA import refusal data for Maria Hernandez 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.