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Eduardo Moreno

⚠️ Moderate Risk

FEI: 3004162834 • Ensenada, Baja California • MEXICO

FEI

FEI Number

3004162834

📍

Location

Ensenada, Baja California

🇲🇽

Country

MEXICO
🏢

Address

Domicilio Conocido Rancho Moreno, , Ensenada, Baja California, Mexico

Moderate Risk

FDA Import Risk Assessment

46.5
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
9/26/2007
Latest Refusal
2/13/2006
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
12.4×10%
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
9/26/2007
24FFB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)
2/13/2006
24FFB08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Eduardo Moreno's FDA import refusal history?

Eduardo Moreno (FEI: 3004162834) has 2 FDA import refusal record(s) in our database, spanning from 2/13/2006 to 9/26/2007.

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. Eduardo Moreno's FEI number is 3004162834.

What types of violations has Eduardo Moreno received?

Eduardo Moreno 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 Eduardo Moreno come from?

All FDA import refusal data for Eduardo Moreno 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.