SONAB CED
⚠️ High Risk
FEI: 3025464057 • Douz, Kebili • TUNISIA
FEI Number
3025464057
Location
Douz, Kebili
Country
TUNISIAAddress
Zone Industrielle Golaa, , Douz, Kebili, Tunisia
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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 |
|---|---|---|---|
| 4/21/2023 | 20GFC99CITRUS FRUIT, N.E.C. | 249FILTHY | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is SONAB CED's FDA import refusal history?
SONAB CED (FEI: 3025464057) has 1 FDA import refusal record(s) in our database, spanning from 4/21/2023 to 4/21/2023.
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. SONAB CED's FEI number is 3025464057.
What types of violations has SONAB CED received?
SONAB CED 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 SONAB CED come from?
All FDA import refusal data for SONAB CED 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.