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Lacompagnie De Kinkiliba

⚠️ Moderate Risk

FEI: 3003994805 • Marville, Meuse • FRANCE

FEI

FEI Number

3003994805

📍

Location

Marville, Meuse

🇫🇷

Country

FRANCE
🏢

Address

1 Zone Industrielle, DE MARVILLE, Marville, Meuse, France

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/16/2009
Latest Refusal
7/16/2009
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
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

113×

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).

Refusal History

DateProductViolationsDivision
7/16/2009
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Southwest Import District Office (SWI-DO)
7/16/2009
36BCT99SYRUPS AND MOLASSES, N.E.C.
11UNSAFE COL
Southwest Import District Office (SWI-DO)
7/16/2009
28BJT54PEPPER, BLACK, GROUND, CRACKED (SPICE)
11UNSAFE COL
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Lacompagnie De Kinkiliba's FDA import refusal history?

Lacompagnie De Kinkiliba (FEI: 3003994805) has 3 FDA import refusal record(s) in our database, spanning from 7/16/2009 to 7/16/2009.

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. Lacompagnie De Kinkiliba's FEI number is 3003994805.

What types of violations has Lacompagnie De Kinkiliba received?

Lacompagnie De Kinkiliba 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 Lacompagnie De Kinkiliba come from?

All FDA import refusal data for Lacompagnie De Kinkiliba 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.