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ALBERTO MANJARREZ DE LA HERRAN

⚠️ Moderate Risk

FEI: 3021716824 • Mazatlan, Sinaloa • MEXICO

FEI

FEI Number

3021716824

📍

Location

Mazatlan, Sinaloa

🇲🇽

Country

MEXICO
🏢

Address

Colonia Centro, Col. Ninos Heroes, Mazatlan, Mazatlan, Sinaloa, Mexico

Moderate Risk

FDA Import Risk Assessment

33.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
3/26/2025
Latest Refusal
3/26/2025
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
11.2×30%
Recency
83.9×20%
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

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
3/26/2025
24FHC12JALAPENO PEPPER, HOT (FRUIT USED AS VEGETABLE)
320LACKS FIRM
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is ALBERTO MANJARREZ DE LA HERRAN's FDA import refusal history?

ALBERTO MANJARREZ DE LA HERRAN (FEI: 3021716824) has 1 FDA import refusal record(s) in our database, spanning from 3/26/2025 to 3/26/2025.

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. ALBERTO MANJARREZ DE LA HERRAN's FEI number is 3021716824.

What types of violations has ALBERTO MANJARREZ DE LA HERRAN received?

ALBERTO MANJARREZ DE LA HERRAN 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 MANJARREZ DE LA HERRAN come from?

All FDA import refusal data for ALBERTO MANJARREZ DE LA HERRAN 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.