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COMERCIALIZADORA MEXICO Y YO SA DE CV

⚠️ Moderate Risk

FEI: 3013355457 • Saltillo, Coahuila de Zaragoza • MEXICO

FEI

FEI Number

3013355457

📍

Location

Saltillo, Coahuila de Zaragoza

🇲🇽

Country

MEXICO
🏢

Address

Periferico Luis Echeverria 1205 Int 17, Col. Avicola, Saltillo, Saltillo, Coahuila de Zaragoza, Mexico

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
6/19/2017
Latest Refusal
6/19/2017
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

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.

2561×

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)).

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

4821×

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.

Refusal History

DateProductViolationsDivision
6/19/2017
30YGT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C.
11UNSAFE COL
249FILTHY
256INCONSPICU
274COLOR LBLG
482NUTRIT LBL
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is COMERCIALIZADORA MEXICO Y YO SA DE CV's FDA import refusal history?

COMERCIALIZADORA MEXICO Y YO SA DE CV (FEI: 3013355457) has 1 FDA import refusal record(s) in our database, spanning from 6/19/2017 to 6/19/2017.

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. COMERCIALIZADORA MEXICO Y YO SA DE CV's FEI number is 3013355457.

What types of violations has COMERCIALIZADORA MEXICO Y YO SA DE CV received?

COMERCIALIZADORA MEXICO Y YO SA DE CV has been cited for 5 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 COMERCIALIZADORA MEXICO Y YO SA DE CV come from?

All FDA import refusal data for COMERCIALIZADORA MEXICO Y YO 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.