ImportRefusal LogoImportRefusal

Rademaker Bv

⚠️ Moderate Risk

FEI: 1000530015 • Culemborg, Gelderland • NETHERLANDS

FEI

FEI Number

1000530015

📍

Location

Culemborg, Gelderland

🇳🇱
🏢

Address

Plantijnweg 23, , Culemborg, Gelderland, Netherlands

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
5/25/2017
Latest Refusal
5/25/2017
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

111×

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).

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
5/25/2017
33EGT02CARAMEL CANDY PIECES, HARD, WITHOUT NUTS OR FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Rademaker Bv's FDA import refusal history?

Rademaker Bv (FEI: 1000530015) has 1 FDA import refusal record(s) in our database, spanning from 5/25/2017 to 5/25/2017.

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. Rademaker Bv's FEI number is 1000530015.

What types of violations has Rademaker Bv received?

Rademaker Bv has been cited for 2 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 Rademaker Bv come from?

All FDA import refusal data for Rademaker Bv 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.