Sea Delight. S.L.
FDA import alert and refusal historySevilla, SpainFEI 3011538395
As of October 26, 2026, Sea Delight. S.L. is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between August 7, 2018 and September 5, 2018, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Anchovy · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sea Delight. S.L.
6 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 3 lines in one entry: Anchovy; Sardines (brisling, sprats, pilchards, etc.)FILTHYEntry 251-2038896-9Show 3 linesHide lines
- Import refusalSource
Refused, 3 lines in one entry: Anchovy; Sardines (brisling, sprats, pilchards, etc.)FILTHYEntry 251-2037700-4Show 3 linesHide lines
Refusal charges, in plain English
- FILTHY6 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Sea Delight. S.L.
- Is Sea Delight. S.L. on an FDA import alert?
- No listing for Sea Delight. S.L. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
- Has FDA refused shipments from Sea Delight. S.L.?
- Yes. FDA refused 6 shipment lines from Sea Delight. S.L. between August 7, 2018 and September 5, 2018. The most recent, on September 5, 2018, was anchovy, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Sea Delight. S.L.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 6 lines).
- What is Sea Delight. S.L.'s FEI number?
- Sea Delight. S.L.'s FDA Establishment Identifier (FEI) is 3011538395.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.