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Grupo GEPP

⚠️ High Risk

FEI: 3012402223 • Cuajilmalpa de Morelos, Cuajilmalpa de Morelos • MEXICO

FEI

FEI Number

3012402223

📍

Location

Cuajilmalpa de Morelos, Cuajilmalpa de Morelos

🇲🇽

Country

MEXICO
🏢

Address

S.A.P.I. de C.V. Av. Santa Fe # 485, Piso 4;Col. Cruz Manca, Cuajilmalpa de Morelos, Cuajilmalpa de Morelos, Mexico

High Risk

FDA Import Risk Assessment

50.3
LowModerateHighCritical

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

Statistics

11
Total Refusals
3
Unique Violations
6/28/2024
Latest Refusal
11/10/2016
Earliest Refusal

Score Breakdown

Violation Severity
64.7×40%
Refusal Volume
40.0×30%
Recency
55.1×20%
Frequency
14.4×10%
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

118×

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).

2744×

COLOR LBLG

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

3243×

NO ENGLISH

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)).

Refusal History

DateProductViolationsDivision
6/28/2024
29BGT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
274COLOR LBLG
Division of Southwest Imports (DSWI)
7/12/2019
29BCT03SOFT DRINK, CORE FRUIT FLAVORED, CARBONATED
11UNSAFE COL
274COLOR LBLG
Division of Southwest Imports (DSWI)
2/28/2018
29BCT09SOFT DRINK, OTHER FRUIT FLAVORED, CARBONATED
11UNSAFE COL
274COLOR LBLG
Division of Southwest Imports (DSWI)
9/18/2017
29BGY02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
274COLOR LBLG
Division of Southwest Imports (DSWI)
8/24/2017
29BHT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
Division of Southwest Imports (DSWI)
8/24/2017
29BHT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
Division of Southwest Imports (DSWI)
2/3/2017
29BGT60SODA WATER, CARBONATED
324NO ENGLISH
Division of Northeast Imports (DNEI)
2/3/2017
29BGT60SODA WATER, CARBONATED
324NO ENGLISH
Division of Northeast Imports (DNEI)
1/13/2017
29BFT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
Division of Northeast Imports (DNEI)
1/13/2017
29BFT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
11UNSAFE COL
Division of Northeast Imports (DNEI)
11/10/2016
29BGT03SOFT DRINK, CORE FRUIT FLAVORED, CARBONATED
324NO ENGLISH
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Grupo GEPP's FDA import refusal history?

Grupo GEPP (FEI: 3012402223) has 11 FDA import refusal record(s) in our database, spanning from 11/10/2016 to 6/28/2024.

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. Grupo GEPP's FEI number is 3012402223.

What types of violations has Grupo GEPP received?

Grupo GEPP 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 Grupo GEPP come from?

All FDA import refusal data for Grupo GEPP 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.