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Deas

FDA import alert and refusal historyKalyves Polygyrou, GreeceFEI 3005784027

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

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As of October 25, 2026, Deas is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 29, 2026, most often for no scheduled process filed (NO PROCESS).

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

Current status

Import alerts
Not listed
Last import refusal
Olives, green, (pit fruit) · NO PROCESS
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Deas

3 records, newest first. Each line links to the FDA page it came from.

2026

  1. Import refusal
    Refused, Olives, green, (pit fruit)NO PROCESSEntry 9PS-1166333-7
    Source

2023

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2016

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • NO PROCESS1 refused line

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Deas

Is Deas on an FDA import alert?
No listing for Deas appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Greece page.
Has FDA refused shipments from Deas?
Yes. FDA refused 1 shipment line from Deas on January 29, 2026. The most recent, on January 29, 2026, was olives, green, (pit fruit), charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Deas's shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
When was Deas last inspected by FDA?
FDA's most recent inspection of Deas with a final classification is dated January 13, 2023 and was classified VAI (Voluntary Action Indicated).
What is Deas's FEI number?
Deas's FDA Establishment Identifier (FEI) is 3005784027.

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Example subjectDea 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.