Goldkenn SA
⚠️ Moderate Risk
FEI: 3009019691 • Le Locle, Neuchatel • SWITZERLAND
FEI Number
3009019691
Location
Le Locle, Neuchatel
Country
SWITZERLANDAddress
Rue James-Pellaton, Case Postale 793, Le Locle, Neuchatel, Switzerland
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
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.
ALCOHOL
The article appears to be a confectionary that bears or contains alcohol in excess of 1/2 of 1% by volume derived solely from the use of flavoring extracts.
NONNUT SUB
The article appears to be confectionery and it bears or contains a nonnutritive substance.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/4/2018 | 34FFT01CHOCOLATE CANDY BAR, WITHOUT NUTS AND FRUIT | 482NUTRIT LBL | Division of Southeast Imports (DSEI) |
| 5/4/2018 | 34GFT01CHOCOLATE CANDY BAR, WITH NUTS AND FRUIT | 482NUTRIT LBL | Division of Southeast Imports (DSEI) |
| 9/22/2016 | 34FGT02CHOCOLATE CANDY PIECES, WITHOUT NUTS AND FRUIT | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Goldkenn SA's FDA import refusal history?
Goldkenn SA (FEI: 3009019691) has 3 FDA import refusal record(s) in our database, spanning from 9/22/2016 to 5/4/2018.
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. Goldkenn SA's FEI number is 3009019691.
What types of violations has Goldkenn SA received?
Goldkenn SA 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 Goldkenn SA come from?
All FDA import refusal data for Goldkenn SA 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.