Chocolaterie De Schutter Nv
⚠️ Moderate Risk
FEI: 3009817915 • Lokeren, Oost-Vlaanderen • BELGIUM
FEI Number
3009817915
Location
Lokeren, Oost-Vlaanderen
Country
BELGIUMAddress
Brandstraat 18, , Lokeren, Oost-Vlaanderen, Belgium
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
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.
USUAL NAME
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(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
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 |
|---|---|---|---|
| 3/16/2012 | 34FGT08CHOCOLATE SUCKERS AND NOVELTIES, WITHOUT NUTS AND FRUIT | Baltimore District Office (BLT-DO) | |
| 3/16/2012 | 34FGT08CHOCOLATE SUCKERS AND NOVELTIES, WITHOUT NUTS AND FRUIT | Baltimore District Office (BLT-DO) | |
| 3/16/2012 | 34FGT08CHOCOLATE SUCKERS AND NOVELTIES, WITHOUT NUTS AND FRUIT | Baltimore District Office (BLT-DO) | |
| 3/16/2012 | 34FGT08CHOCOLATE SUCKERS AND NOVELTIES, WITHOUT NUTS AND FRUIT | Baltimore District Office (BLT-DO) | |
| 3/16/2012 | 34FGT08CHOCOLATE SUCKERS AND NOVELTIES, WITHOUT NUTS AND FRUIT | Baltimore District Office (BLT-DO) | |
| 3/12/2012 | 34KGT04CHOCOLATE BARS | Baltimore District Office (BLT-DO) | |
| 3/12/2012 | 34KGT04CHOCOLATE BARS | Baltimore District Office (BLT-DO) | |
| 3/12/2012 | 34KGT04CHOCOLATE BARS | Baltimore District Office (BLT-DO) | |
| 3/12/2012 | 34KGT04CHOCOLATE BARS | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Chocolaterie De Schutter Nv's FDA import refusal history?
Chocolaterie De Schutter Nv (FEI: 3009817915) has 9 FDA import refusal record(s) in our database, spanning from 3/12/2012 to 3/16/2012.
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. Chocolaterie De Schutter Nv's FEI number is 3009817915.
What types of violations has Chocolaterie De Schutter Nv received?
Chocolaterie De Schutter Nv has been cited for 5 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 Chocolaterie De Schutter Nv come from?
All FDA import refusal data for Chocolaterie De Schutter Nv 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.