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Sogelma (AKA El Kadira S.A.)

FDA import alert and refusal historyMeknes, MoroccoFEI 3003048031

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Example subjectSogelma (AKA El Kadira S.A. added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sogelma (AKA El Kadira S.A.) (Meknes, Morocco) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for frozen strawberries, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Sogelma (AKA El Kadira S.A.)

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

2009

  1. Import alert listing
    Listed on Import Alert 99-08red listFrozen strawberries
    Source

Questions about Sogelma (AKA El Kadira S.A.)

Is Sogelma (AKA El Kadira S.A.) on an FDA import alert?
Yes. As of October 26, 2026, Sogelma (AKA El Kadira S.A.) is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for frozen strawberries; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Sogelma (AKA El Kadira S.A.)?
No FDA import refusals for Sogelma (AKA El Kadira S.A.) appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Sogelma (AKA El Kadira S.A.)'s FEI number?
Sogelma (AKA El Kadira S.A.)'s FDA Establishment Identifier (FEI) is 3003048031.
Can shipments from Sogelma (AKA El Kadira S.A.) still enter the U.S.?
Shipments of frozen strawberries from Sogelma (AKA El Kadira S.A.) can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectSogelma (AKA El Kadira 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.