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JOSE BENIGNO OSORIO OROPEZA

⚠️ High Risk

FEI: 3028663338 • Quecholac, PUE • MEXICO

FEI

FEI Number

3028663338

📍

Location

Quecholac, PUE

🇲🇽

Country

MEXICO
🏢

Address

C.8 Norte 613 San Simon, , Quecholac, PUE, Mexico

High Risk

FDA Import Risk Assessment

66.8
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

2
Total Refusals
1
Unique Violations
12/3/2025
Latest Refusal
12/3/2025
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
97.7×20%
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

2412×

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
12/3/2025
24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)
12/3/2025
24FFC08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is JOSE BENIGNO OSORIO OROPEZA's FDA import refusal history?

JOSE BENIGNO OSORIO OROPEZA (FEI: 3028663338) has 2 FDA import refusal record(s) in our database, spanning from 12/3/2025 to 12/3/2025.

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. JOSE BENIGNO OSORIO OROPEZA's FEI number is 3028663338.

What types of violations has JOSE BENIGNO OSORIO OROPEZA received?

JOSE BENIGNO OSORIO OROPEZA 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 JOSE BENIGNO OSORIO OROPEZA come from?

All FDA import refusal data for JOSE BENIGNO OSORIO OROPEZA 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.