Denia Ltd
⚠️ Moderate Risk
FEI: 3001681465 • Sofia • BULGARIA
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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/24/2002 | 25PHC07MUSHROOM, CHANTERELLE, WHOLE (BUTTON) (FUNGI) | 249FILTHY | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Denia Ltd's FDA import refusal history?
Denia Ltd (FEI: 3001681465) has 1 FDA import refusal record(s) in our database, spanning from 7/24/2002 to 7/24/2002.
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. Denia Ltd's FEI number is 3001681465.
What types of violations has Denia Ltd received?
Denia Ltd 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 Denia Ltd come from?
All FDA import refusal data for Denia Ltd 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.