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JUAN ANTONIO IBARRA CARDENAS

⚠️ Moderate Risk

FEI: 3011557329 • Villa de Arista, San Luis Potosi • MEXICO

FEI

FEI Number

3011557329

📍

Location

Villa de Arista, San Luis Potosi

🇲🇽

Country

MEXICO
🏢

Address

Calle Cuauhtemoc 410, Col. VILLA DE ARISTA, Villa de Arista, San Luis Potosi, Mexico

Moderate Risk

FDA Import Risk Assessment

40.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
8/20/2015
Latest Refusal
8/20/2015
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
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

3061×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

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
8/20/2015
24TFC46CILANTRO (LEAF & STEM VEGETABLE)
306INSANITARY
308MFR INSAN
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is JUAN ANTONIO IBARRA CARDENAS's FDA import refusal history?

JUAN ANTONIO IBARRA CARDENAS (FEI: 3011557329) has 1 FDA import refusal record(s) in our database, spanning from 8/20/2015 to 8/20/2015.

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. JUAN ANTONIO IBARRA CARDENAS's FEI number is 3011557329.

What types of violations has JUAN ANTONIO IBARRA CARDENAS received?

JUAN ANTONIO IBARRA CARDENAS 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 JUAN ANTONIO IBARRA CARDENAS come from?

All FDA import refusal data for JUAN ANTONIO IBARRA CARDENAS 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.