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GRUPO JUMEX SA DE CV

⚠️ Moderate Risk

FEI: 3024652988 • Mexico Df • MEXICO

FEI

FEI Number

3024652988

📍

Location

Mexico Df

🇲🇽

Country

MEXICO
🏢

Address

Ecatepec De Morelos, , Mexico Df, , Mexico

Moderate Risk

FDA Import Risk Assessment

49.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
3/26/2025
Latest Refusal
3/26/2025
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
83.8×20%
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

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

2601×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

Refusal History

DateProductViolationsDivision
3/26/2025
21VCT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
238UNSAFE ADD
260FALSE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is GRUPO JUMEX SA DE CV's FDA import refusal history?

GRUPO JUMEX SA DE CV (FEI: 3024652988) has 1 FDA import refusal record(s) in our database, spanning from 3/26/2025 to 3/26/2025.

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. GRUPO JUMEX SA DE CV's FEI number is 3024652988.

What types of violations has GRUPO JUMEX SA DE CV received?

GRUPO JUMEX SA DE CV has been cited for 2 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 JUMEX SA DE CV come from?

All FDA import refusal data for GRUPO JUMEX 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.