Sea Delight. S.L.
⚠️ High Risk
FEI: 3011538395 • Sevilla, Sevilla • SPAIN
FEI Number
3011538395
Location
Sevilla, Sevilla
Country
SPAINAddress
Torre, Calle Arquitectura 1, Sevilla, Sevilla, Spain
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 |
|---|---|---|---|
| 9/5/2018 | 16AGP01ANCHOVY | 249FILTHY | Division of Northeast Imports (DNEI) |
| 9/5/2018 | 16AGP33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 249FILTHY | Division of Northeast Imports (DNEI) |
| 9/5/2018 | 16AGP01ANCHOVY | 249FILTHY | Division of Northeast Imports (DNEI) |
| 8/7/2018 | 16AGP01ANCHOVY | 249FILTHY | Division of Northeast Imports (DNEI) |
| 8/7/2018 | 16AGP33SARDINES (BRISLING, SPRATS, PILCHARDS, ETC.) | 249FILTHY | Division of Northeast Imports (DNEI) |
| 8/7/2018 | 16AGP01ANCHOVY | 249FILTHY | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Sea Delight. S.L.'s FDA import refusal history?
Sea Delight. S.L. (FEI: 3011538395) has 6 FDA import refusal record(s) in our database, spanning from 8/7/2018 to 9/5/2018.
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. Sea Delight. S.L.'s FEI number is 3011538395.
What types of violations has Sea Delight. S.L. received?
Sea Delight. S.L. 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 Sea Delight. S.L. come from?
All FDA import refusal data for Sea Delight. S.L. 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.