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Kempico C.V.

⚠️ Moderate Risk

FEI: 3004305690 • Gierle, Antwerp • BELGIUM

FEI

FEI Number

3004305690

📍

Location

Gierle, Antwerp

🇧🇪

Country

BELGIUM
🏢

Address

Melkerijstraat 1, , Gierle, Antwerp, Belgium

Moderate Risk

FDA Import Risk Assessment

47.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
3/18/2013
Latest Refusal
5/15/2012
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

2384×

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.

Refusal History

DateProductViolationsDivision
3/18/2013
12AVO52CHEESE, SEMISOFT
238UNSAFE ADD
Division of Northeast Imports (DNEI)
1/9/2013
12AVO52CHEESE, SEMISOFT
238UNSAFE ADD
Division of Northeast Imports (DNEI)
1/3/2013
12AVO52CHEESE, SEMISOFT
238UNSAFE ADD
Division of Northeast Imports (DNEI)
5/15/2012
12AGP52CHEESE, SEMISOFT
238UNSAFE ADD
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Kempico C.V.'s FDA import refusal history?

Kempico C.V. (FEI: 3004305690) has 4 FDA import refusal record(s) in our database, spanning from 5/15/2012 to 3/18/2013.

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. Kempico C.V.'s FEI number is 3004305690.

What types of violations has Kempico C.V. received?

Kempico C.V. 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 Kempico C.V. come from?

All FDA import refusal data for Kempico C.V. 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.