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Dr. Oetker Nederland b.v.

⚠️ Moderate Risk

FEI: 3007116011 • TE Amersfoort • NETHERLANDS

FEI

FEI Number

3007116011

📍

Location

TE Amersfoort

🇳🇱
🏢

Address

Antwoordnummer 7204, , TE Amersfoort, , 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
12/1/2008
Latest Refusal
12/1/2008
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
12/1/2008
03PFT04PIES AND PUDDING PREPARED DRY MIX WITH CUSTARD OR CREAM FILLING
11UNSAFE COL
482NUTRIT LBL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Dr. Oetker Nederland b.v.'s FDA import refusal history?

Dr. Oetker Nederland b.v. (FEI: 3007116011) has 1 FDA import refusal record(s) in our database, spanning from 12/1/2008 to 12/1/2008.

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. Dr. Oetker Nederland b.v.'s FEI number is 3007116011.

What types of violations has Dr. Oetker Nederland b.v. received?

Dr. Oetker Nederland b.v. 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 Dr. Oetker Nederland b.v. come from?

All FDA import refusal data for Dr. Oetker Nederland b.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.