Olam Ivoire SA
FDA import alert and refusal historyAbidjan, Cote d'IvoireFEI 3017530065
As of October 26, 2026, Olam Ivoire SA is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between November 12, 2021 and May 6, 2022, most often for salmonella (SALMONELLA).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cashew, shelled · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Olam Ivoire SA
5 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Cashew, shelledSALMONELLAEntry 609-0610602-0Source
- Import refusalRefused, Cashew, shelledSALMONELLAEntry 609-0608528-1Source
- Import refusalRefused, Cashew, shelledSALMONELLAEntry 609-0610985-9Source
2021
- Import refusalRefused, Cashew, shelledSALMONELLAEntry 609-0608853-3Source
- Import refusalRefused, Cashew, shelledSALMONELLAEntry 609-0607109-1Source
Refusal charges, in plain English
- SALMONELLA5 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Olam Ivoire SA
- Is Olam Ivoire SA on an FDA import alert?
- No listing for Olam Ivoire SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Cote d'Ivoire page.
- Has FDA refused shipments from Olam Ivoire SA?
- Yes. FDA refused 5 shipment lines from Olam Ivoire SA between November 12, 2021 and May 6, 2022. The most recent, on May 6, 2022, was cashew, shelled, charged as SALMONELLA (salmonella).
- Why did FDA refuse Olam Ivoire SA's shipments?
- The most frequent charge is SALMONELLA (salmonella, 5 lines).
- What is Olam Ivoire SA's FEI number?
- Olam Ivoire SA's FDA Establishment Identifier (FEI) is 3017530065.
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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.