Royal Unibrew A/S
⚠️ Moderate Risk
FEI: 3004332782 • Faxe, DK-NOTA • DENMARK
FEI Number
3004332782
Location
Faxe, DK-NOTA
Country
DENMARKAddress
Faxe Alle 1, , Faxe, DK-NOTA, Denmark
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
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 |
|---|---|---|---|
| 4/18/2014 | 29BCY99CARBONATED SOFT DRINK, N.E.C. | 11UNSAFE COL | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Royal Unibrew A/S's FDA import refusal history?
Royal Unibrew A/S (FEI: 3004332782) has 1 FDA import refusal record(s) in our database, spanning from 4/18/2014 to 4/18/2014.
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. Royal Unibrew A/S's FEI number is 3004332782.
What types of violations has Royal Unibrew A/S received?
Royal Unibrew A/S has been cited for 1 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 Royal Unibrew A/S come from?
All FDA import refusal data for Royal Unibrew A/S 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.