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ROBERTO MADRID PADILLA

⚠️ Moderate Risk

FEI: 2000045989 • Tijuana, Baja California • MEXICO

FEI

FEI Number

2000045989

📍

Location

Tijuana, Baja California

🇲🇽

Country

MEXICO
🏢

Address

Calle Mariscal Sucre 65 D, Col. Las Huertas 3ra Secc, Tijuana, Tijuana, Baja California, 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
8/15/2011
Latest Refusal
8/15/2011
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
8/15/2011
21SFC06PAPAYA (PAPAW) (SUBTROPICAL AND TROPICAL FRUIT)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is ROBERTO MADRID PADILLA's FDA import refusal history?

ROBERTO MADRID PADILLA (FEI: 2000045989) has 1 FDA import refusal record(s) in our database, spanning from 8/15/2011 to 8/15/2011.

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. ROBERTO MADRID PADILLA's FEI number is 2000045989.

What types of violations has ROBERTO MADRID PADILLA received?

ROBERTO MADRID PADILLA 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 ROBERTO MADRID PADILLA come from?

All FDA import refusal data for ROBERTO MADRID PADILLA 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.