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Suria Abdelrahman

FDA import alert and refusal historyCairo, EgyptFEI 3043949649

Recorded by FDA as SURIA ABDELRAHMAN

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Example subjectSuria Abdelrahma added to Import Alert 16-129 (red list)

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As of October 26, 2026, Suria Abdelrahman is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 15, 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
Tamarind (subtropical and tropical fruit) · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Suria Abdelrahman

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

2026

  1. Import refusal
    Refused, Tamarind (subtropical and tropical fruit)FILTHYEntry 1FX-6918633-5
    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 Suria Abdelrahman

Is Suria Abdelrahman on an FDA import alert?
No listing for Suria Abdelrahman appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Egypt page.
Has FDA refused shipments from Suria Abdelrahman?
Yes. FDA refused 1 shipment line from Suria Abdelrahman on May 15, 2026. The most recent, on May 15, 2026, was tamarind (subtropical and tropical fruit), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Suria Abdelrahman's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Suria Abdelrahman's FEI number?
Suria Abdelrahman's FDA Establishment Identifier (FEI) is 3043949649.

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Example subjectSuria Abdelrahma 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.