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Polizoidou Anastasia

FDA import alert and refusal historyAlexandroupoli, GreeceFEI 3015859557

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

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As of October 26, 2026, Polizoidou Anastasia is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 6, 2025, most often for listeria monocytogenes (LISTERIA).

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

Current status

Import alerts
Not listed
Last import refusal
Sesame seed paste (e.g., tahina), edible seed prod. · LISTERIA
Last warning letter
None found
Last inspection
None on record

Every FDA record for Polizoidou Anastasia

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

2025

  1. Import refusal
    Refused, Sesame seed paste (e.g., tahina), edible seed prod.LISTERIAEntry 024-1672161-7
    Source

Refusal charges, in plain English

  • LISTERIA1 refused line

    Listeria monocytogenes

    The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Polizoidou Anastasia

Is Polizoidou Anastasia on an FDA import alert?
No listing for Polizoidou Anastasia appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Greece page.
Has FDA refused shipments from Polizoidou Anastasia?
Yes. FDA refused 1 shipment line from Polizoidou Anastasia on March 6, 2025. The most recent, on March 6, 2025, was sesame seed paste (e.g., tahina), edible seed prod., charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse Polizoidou Anastasia's shipments?
The most frequent charge is LISTERIA (listeria monocytogenes, 1 line).
What is Polizoidou Anastasia's FEI number?
Polizoidou Anastasia's FDA Establishment Identifier (FEI) is 3015859557.

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Example subjectPolizoidou Anastasi 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.