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De Ruijter Bv

⚠️ Moderate Risk

FEI: 3009866373 • Zeist, Utrecht • NETHERLANDS

FEI

FEI Number

3009866373

📍

Location

Zeist, Utrecht

🇳🇱
🏢

Address

Postbus 397, , Zeist, Utrecht, Netherlands

Moderate Risk

FDA Import Risk Assessment

32.5
LowModerateHighCritical

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

Statistics

9
Total Refusals
3
Unique Violations
5/31/2013
Latest Refusal
5/10/2013
Earliest Refusal

Score Breakdown

Violation Severity
30.9×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

3249×

NO ENGLISH

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

3211×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

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
5/31/2013
34KFT07CHOCOLATE CHUNKS
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/31/2013
33TFT99TOPPINGS WITHOUT FRUIT, NUTS OR CHOCOLATE N.E.C.
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/31/2013
34KFT07CHOCOLATE CHUNKS
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/31/2013
34KFT01CHOCOLATE CHIPS
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/31/2013
34KFT01CHOCOLATE CHIPS
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/31/2013
34KFT01CHOCOLATE CHIPS
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/31/2013
34KFT01CHOCOLATE CHIPS
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/31/2013
34KFT01CHOCOLATE CHIPS
324NO ENGLISH
New Orleans District Office (NOL-DO)
5/10/2013
33SFT01CAKE DECORATION (WITHOUT CHOCOLATE)
321LACKS N/C
324NO ENGLISH
482NUTRIT LBL
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is De Ruijter Bv's FDA import refusal history?

De Ruijter Bv (FEI: 3009866373) has 9 FDA import refusal record(s) in our database, spanning from 5/10/2013 to 5/31/2013.

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. De Ruijter Bv's FEI number is 3009866373.

What types of violations has De Ruijter Bv received?

De Ruijter Bv has been cited for 3 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 De Ruijter Bv come from?

All FDA import refusal data for De Ruijter 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.