ImportRefusal LogoImportRefusal

F-Diaz de Mexico, S.A. de C.V.

⚠️ High Risk

FEI: 3035159346 • Aguascalientes, Aguascalientes • MEXICO

FEI

FEI Number

3035159346

📍

Location

Aguascalientes, Aguascalientes

🇲🇽

Country

MEXICO
🏢

Address

Carr. Estatal 52 Cereso - Jesus Maria Km 2 A, , Aguascalientes, Aguascalientes, Mexico

High Risk

FDA Import Risk Assessment

62.1
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

1
Total Refusals
1
Unique Violations
6/27/2025
Latest Refusal
6/27/2025
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
89.0×20%
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

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

Refusal History

DateProductViolationsDivision
6/27/2025
21VGT14TAMARIND, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
249FILTHY
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is F-Diaz de Mexico, S.A. de C.V.'s FDA import refusal history?

F-Diaz de Mexico, S.A. de C.V. (FEI: 3035159346) has 1 FDA import refusal record(s) in our database, spanning from 6/27/2025 to 6/27/2025.

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. F-Diaz de Mexico, S.A. de C.V.'s FEI number is 3035159346.

What types of violations has F-Diaz de Mexico, S.A. de C.V. received?

F-Diaz de Mexico, S.A. de C.V. 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 F-Diaz de Mexico, S.A. de C.V. come from?

All FDA import refusal data for F-Diaz de Mexico, S.A. de C.V. 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.