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LA SUERTE

⚠️ High Risk

FEI: 3027629245 • Trujillo, Valle Del Cauca • COLOMBIA

FEI

FEI Number

3027629245

📍

Location

Trujillo, Valle Del Cauca

🇨🇴

Country

COLOMBIA
🏢

Address

Vereda Bohemia, , Trujillo, Valle Del Cauca, Colombia

High Risk

FDA Import Risk Assessment

60.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/13/2024
Latest Refusal
5/8/2024
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
22.3×30%
Recency
51.6×20%
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

2413×

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
5/13/2024
20GFC05LIME (CITRUS)
241PESTICIDE
Division of Northeast Imports (DNEI)
5/9/2024
20GFC05LIME (CITRUS)
241PESTICIDE
Division of Southeast Imports (DSEI)
5/8/2024
20GFC05LIME (CITRUS)
241PESTICIDE
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is LA SUERTE's FDA import refusal history?

LA SUERTE (FEI: 3027629245) has 3 FDA import refusal record(s) in our database, spanning from 5/8/2024 to 5/13/2024.

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. LA SUERTE's FEI number is 3027629245.

What types of violations has LA SUERTE received?

LA SUERTE 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 LA SUERTE come from?

All FDA import refusal data for LA SUERTE 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.