DE RUIJTER
⚠️ Moderate Risk
FEI: 3003410120 • BAARN, Utrecht • NETHERLANDS
FEI Number
3003410120
Location
BAARN, Utrecht
Country
NETHERLANDSAddress
DE BROODVERSIERDER, POSTBUS 161, BAARN, Utrecht, Netherlands
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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)).
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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/15/2013 | 33SFT01CAKE DECORATION (WITHOUT CHOCOLATE) | New Orleans District Office (NOL-DO) | |
| 4/15/2013 | 34KFT01CHOCOLATE CHIPS | New Orleans District Office (NOL-DO) | |
| 4/15/2013 | 34KFT01CHOCOLATE CHIPS | New Orleans District Office (NOL-DO) | |
| 3/4/2013 | 34KFT01CHOCOLATE CHIPS | New Orleans District Office (NOL-DO) | |
| 3/4/2013 | 28BFT03ANISE (STAR ANISE), GROUND, CRACKED (SPICE) | New Orleans District Office (NOL-DO) | |
| 3/4/2013 | 03AGT03BISCUITS | New Orleans District Office (NOL-DO) | |
| 3/4/2013 | 03AGT03BISCUITS | New Orleans District Office (NOL-DO) | |
| 9/17/2007 | 33SFT99CANDY SPECIALTIES, N.E.C. (WITHOUT CHOCOLATE) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is DE RUIJTER's FDA import refusal history?
DE RUIJTER (FEI: 3003410120) has 8 FDA import refusal record(s) in our database, spanning from 9/17/2007 to 4/15/2013.
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's FEI number is 3003410120.
What types of violations has DE RUIJTER received?
DE RUIJTER 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 come from?
All FDA import refusal data for DE RUIJTER 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.