ImportRefusal LogoImportRefusal

EL TEXANO INTERNACIONAL SA DE CV

⚠️ Moderate Risk

FEI: 3015497744 • Ciudad Santa Catarina, Nuevo Leon • MEXICO

FEI

FEI Number

3015497744

📍

Location

Ciudad Santa Catarina, Nuevo Leon

🇲🇽

Country

MEXICO
🏢

Address

Calle Dionisio De Herrera # 1500 Int. A, Col. Zimix, Santa Catarina, Ciudad Santa Catarina, Nuevo Leon, Mexico

Moderate Risk

FDA Import Risk Assessment

43.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
7/11/2025
Latest Refusal
5/13/2025
Earliest Refusal

Score Breakdown

Violation Severity
48.0×40%
Refusal Volume
22.3×30%
Recency
75.1×20%
Frequency
30.0×10%
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

2562×

INCONSPICU

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

4822×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

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
7/11/2025
20AGH10RAISINS (DRIED GRAPES) (BERRY)
249FILTHY
Division of Southwest Imports (DSWI)
5/13/2025
23KGT01PUMPKIN SEED (EDIBLE SEED)
256INCONSPICU
482NUTRIT LBL
Division of Southwest Imports (DSWI)
5/13/2025
23KGT02SESAME SEED (EDIBLE SEED)
256INCONSPICU
482NUTRIT LBL
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is EL TEXANO INTERNACIONAL SA DE CV's FDA import refusal history?

EL TEXANO INTERNACIONAL SA DE CV (FEI: 3015497744) has 3 FDA import refusal record(s) in our database, spanning from 5/13/2025 to 7/11/2025.

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. EL TEXANO INTERNACIONAL SA DE CV's FEI number is 3015497744.

What types of violations has EL TEXANO INTERNACIONAL SA DE CV received?

EL TEXANO INTERNACIONAL SA DE CV has been cited for 3 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 EL TEXANO INTERNACIONAL SA DE CV come from?

All FDA import refusal data for EL TEXANO INTERNACIONAL 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.