SupplierRadar

Margafrique

FDA import alert and refusal historyCasablanca, MoroccoFEI 3013227669

Recorded by FDA as MARGAFRIQUE

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

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As of October 26, 2026, Margafrique is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 24, 2022, most often for importer not in compliance with fsvp (FSVP VIO).

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

Current status

Import alerts
Not listed
Last import refusal
Filled milk, cheese type product · FSVP VIO
Last warning letter
None found
Last inspection
None on record

Every FDA record for Margafrique

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

2022

  1. Import refusal
    Refused, Filled milk, cheese type productFSVP VIOEntry 551-0468121-5
    Source

Refusal charges, in plain English

  • FSVP VIO1 refused line

    Importer not in compliance with FSVP

    The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.

Questions about Margafrique

Is Margafrique on an FDA import alert?
No listing for Margafrique appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Morocco page.
Has FDA refused shipments from Margafrique?
Yes. FDA refused 1 shipment line from Margafrique on February 24, 2022. The most recent, on February 24, 2022, was filled milk, cheese type product, charged as FSVP VIO (importer not in compliance with fsvp).
Why did FDA refuse Margafrique's shipments?
The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 1 line).
What is Margafrique's FEI number?
Margafrique's FDA Establishment Identifier (FEI) is 3013227669.

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Example subjectMargafriqu 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.