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C I Trandex Itda

⚠️ Moderate Risk

FEI: 3005098410 • Palmira • COLOMBIA

FEI

FEI Number

3005098410

📍

Location

Palmira

🇨🇴

Country

COLOMBIA
🏢

Address

Calle 58# 27a-22, , Palmira, , Colombia

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
6/28/2005
Latest Refusal
6/28/2005
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

832×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
6/28/2005
24VCT01ARTICHOKE, WITH SAUCE
83NO PROCESS
New Orleans District Office (NOL-DO)
6/28/2005
24HCH50TOMATO, DRIED
83NO PROCESS
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is C I Trandex Itda's FDA import refusal history?

C I Trandex Itda (FEI: 3005098410) has 2 FDA import refusal record(s) in our database, spanning from 6/28/2005 to 6/28/2005.

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. C I Trandex Itda's FEI number is 3005098410.

What types of violations has C I Trandex Itda received?

C I Trandex Itda 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 C I Trandex Itda come from?

All FDA import refusal data for C I Trandex Itda 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.