Societe Hongsheng Maoyi Gongsi Sarl
FDA import alert and refusal historyAbidjan, Cote d'IvoireFEI 3032447136
Recorded by FDA as SOCIETE HONGSHENG MAOYI GONGSI SARL
As of October 27, 2026, Societe Hongsheng Maoyi Gongsi Sarl is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between January 10, 2025 and October 7, 2026, 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 Societe Hongsheng Maoyi Gongsi Sarl
4 records, newest first. Each line links to the FDA page it came from.
2026
2025
Refusal charges, in plain English
- FILTHY4 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 Societe Hongsheng Maoyi Gongsi Sarl
- Is Societe Hongsheng Maoyi Gongsi Sarl on an FDA import alert?
- No listing for Societe Hongsheng Maoyi Gongsi Sarl appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Cote d'Ivoire page.
- Has FDA refused shipments from Societe Hongsheng Maoyi Gongsi Sarl?
- Yes. FDA refused 4 shipment lines from Societe Hongsheng Maoyi Gongsi Sarl between January 10, 2025 and October 7, 2026. The most recent, on October 7, 2026, was fish maw, fishery products, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Societe Hongsheng Maoyi Gongsi Sarl's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 4 lines).
- What is Societe Hongsheng Maoyi Gongsi Sarl's FEI number?
- Societe Hongsheng Maoyi Gongsi Sarl's FDA Establishment Identifier (FEI) is 3032447136.
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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.