ImportRefusal LogoImportRefusal

Alberto Hernandez Montero

⚠️ Moderate Risk

FEI: 3007574941 • Oaxaca De Juarez, Oaxaca • MEXICO

FEI

FEI Number

3007574941

📍

Location

Oaxaca De Juarez, Oaxaca

🇲🇽

Country

MEXICO
🏢

Address

Calle Queretaro # 44, Fracc. Elsa, Oaxaca De Juarez, Oaxaca De Juarez, Oaxaca, 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
2/10/2015
Latest Refusal
2/10/2015
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
2/10/2015
21SFC07PINEAPPLE (SUBTROPICAL AND TROPICAL FRUIT)
241PESTICIDE
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Alberto Hernandez Montero's FDA import refusal history?

Alberto Hernandez Montero (FEI: 3007574941) has 1 FDA import refusal record(s) in our database, spanning from 2/10/2015 to 2/10/2015.

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. Alberto Hernandez Montero's FEI number is 3007574941.

What types of violations has Alberto Hernandez Montero received?

Alberto Hernandez Montero 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 Alberto Hernandez Montero come from?

All FDA import refusal data for Alberto Hernandez Montero 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.