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Manzela Sa De Cv

⚠️ Moderate Risk

FEI: 3001388105 • Pueblo San Pedro Cuautlalpan, Mexico • MEXICO

FEI

FEI Number

3001388105

📍

Location

Pueblo San Pedro Cuautlalpan, Mexico

🇲🇽

Country

MEXICO
🏢

Address

Ampuero Lote 29 Mz 17 Fraccionamiento, Texcoco, Pueblo San Pedro Cuautlalpan, Mexico, Mexico

Moderate Risk

FDA Import Risk Assessment

45.3
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
4/15/2004
Latest Refusal
2/13/2003
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
25.6×10%
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

2973×

AFLATOXIN

The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
4/15/2004
23BGT07PEANUT, SHELLED
297AFLATOXIN
Southwest Import District Office (SWI-DO)
2/11/2004
33AGT99HARD CANDY WITH NUT OR NUT PRODUCTS, N.E.C. (WITHOUT CHOCOLATE)
297AFLATOXIN
Southwest Import District Office (SWI-DO)
2/13/2003
23BGT07PEANUT, SHELLED
297AFLATOXIN
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Manzela Sa De Cv's FDA import refusal history?

Manzela Sa De Cv (FEI: 3001388105) has 3 FDA import refusal record(s) in our database, spanning from 2/13/2003 to 4/15/2004.

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. Manzela Sa De Cv's FEI number is 3001388105.

What types of violations has Manzela Sa De Cv received?

Manzela Sa De Cv 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 Manzela Sa De Cv come from?

All FDA import refusal data for Manzela Sa De Cv 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.