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Produits Des Iles S.A.

FDA import alert and refusal historyDelmas, HaitiFEI 3012269606

Recorded by FDA as PRODUITS DES ILES S.A.

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Example subjectProduits Des Iles S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Produits Des Iles S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 11, 2016, 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
Cocoa bean n.e.c. · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Produits Des Iles S.A.

1 record, newest first. Each line links to the FDA page it came from.

2016

  1. Import refusal
    Refused, Cocoa bean n.e.c.FILTHYEntry 238-1032475-8
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    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 Produits Des Iles S.A.

Is Produits Des Iles S.A. on an FDA import alert?
No listing for Produits Des Iles S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Haiti page.
Has FDA refused shipments from Produits Des Iles S.A.?
Yes. FDA refused 1 shipment line from Produits Des Iles S.A. on October 11, 2016. The most recent, on October 11, 2016, was cocoa bean n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Produits Des Iles S.A.'s shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Produits Des Iles S.A.'s FEI number?
Produits Des Iles S.A.'s FDA Establishment Identifier (FEI) is 3012269606.

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Example subjectProduits Des Iles S.A added to Import Alert 16-129 (red list)

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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.