Ets Souleymane Gningue Import Export
FDA import alert and refusal historyDakar, SenegalFEI 3011384126
Recorded by FDA as ETS SOULEYMANE GNINGUE IMPORT EXPORT
As of October 26, 2026, Ets Souleymane Gningue Import Export is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between September 13, 2018 and May 17, 2022, 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
- Fish maw, fishery products, n.e.c. · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ets Souleymane Gningue Import Export
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY2 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 Ets Souleymane Gningue Import Export
- Is Ets Souleymane Gningue Import Export on an FDA import alert?
- No listing for Ets Souleymane Gningue Import Export appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Senegal page.
- Has FDA refused shipments from Ets Souleymane Gningue Import Export?
- Yes. FDA refused 2 shipment lines from Ets Souleymane Gningue Import Export between September 13, 2018 and May 17, 2022. The most recent, on May 17, 2022, was fish maw, fishery products, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Ets Souleymane Gningue Import Export's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Ets Souleymane Gningue Import Export's FEI number?
- Ets Souleymane Gningue Import Export's FDA Establishment Identifier (FEI) is 3011384126.
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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.