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LIMONES MONICA SA DE CV

⚠️ Moderate Risk

FEI: 3010106286 • Martinez De La Torre, Veracruz de Ignacio de La Llav • MEXICO

FEI

FEI Number

3010106286

📍

Location

Martinez De La Torre, Veracruz de Ignacio de La Llav

🇲🇽

Country

MEXICO
🏢

Address

Gregorio Torres Quintero Sn, , Martinez De La Torre, Veracruz de Ignacio de La Llav, Mexico

Moderate Risk

FDA Import Risk Assessment

49.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/18/2022
Latest Refusal
11/18/2022
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
11.2×30%
Recency
23.0×20%
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

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
11/18/2022
20GFC05LIME (CITRUS)
241PESTICIDE
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is LIMONES MONICA SA DE CV's FDA import refusal history?

LIMONES MONICA SA DE CV (FEI: 3010106286) has 1 FDA import refusal record(s) in our database, spanning from 11/18/2022 to 11/18/2022.

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. LIMONES MONICA SA DE CV's FEI number is 3010106286.

What types of violations has LIMONES MONICA SA DE CV received?

LIMONES MONICA SA DE CV 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 LIMONES MONICA SA DE CV come from?

All FDA import refusal data for LIMONES MONICA 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.