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DEFRUT S.A. DE C.V.

⚠️ Moderate Risk

FEI: 3004856519 • Morelia, MX-MIC • MEXICO

FEI

FEI Number

3004856519

📍

Location

Morelia, MX-MIC

🇲🇽

Country

MEXICO
🏢

Address

Km. 323.5 Carr. Mexico-Guadalajara, Col. Avicola, Morelia, MX-MIC, Mexico

Moderate Risk

FDA Import Risk Assessment

45.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
5/20/2014
Latest Refusal
12/27/2006
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
2.7×10%
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

2492×

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
5/20/2014
21TGT14TAMARIND, DRIED OR PASTE
249FILTHY
Southwest Import District Office (SWI-DO)
12/27/2006
37BDH28BEAN CURD, DRIED (STICKS, SHEETS), (MULTIPLE FOOD SPECIALTIES, SIDE DISHES AND DESSERTS
249FILTHY
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is DEFRUT S.A. DE C.V.'s FDA import refusal history?

DEFRUT S.A. DE C.V. (FEI: 3004856519) has 2 FDA import refusal record(s) in our database, spanning from 12/27/2006 to 5/20/2014.

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. DEFRUT S.A. DE C.V.'s FEI number is 3004856519.

What types of violations has DEFRUT S.A. DE C.V. received?

DEFRUT 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 DEFRUT S.A. DE C.V. come from?

All FDA import refusal data for DEFRUT 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.