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ROBERTO MARIO ALARCON MONTELONGO

⚠️ Moderate Risk

FEI: 3004390311 • Reynosa, Tamaulipas • MEXICO

FEI

FEI Number

3004390311

📍

Location

Reynosa, Tamaulipas

🇲🇽

Country

MEXICO
🏢

Address

Calle Camino Real # 700, Col. Esfuerzo Nacional, Reynosa, Reynosa, Tamaulipas, 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
3/2/2005
Latest Refusal
3/2/2005
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
3/2/2005
24THC99LEAF & STEM VEGETABLES, N.E.C.
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is ROBERTO MARIO ALARCON MONTELONGO's FDA import refusal history?

ROBERTO MARIO ALARCON MONTELONGO (FEI: 3004390311) has 1 FDA import refusal record(s) in our database, spanning from 3/2/2005 to 3/2/2005.

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 MARIO ALARCON MONTELONGO's FEI number is 3004390311.

What types of violations has ROBERTO MARIO ALARCON MONTELONGO received?

ROBERTO MARIO ALARCON MONTELONGO 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 MARIO ALARCON MONTELONGO come from?

All FDA import refusal data for ROBERTO MARIO ALARCON MONTELONGO 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.