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Argos Fortuna Sp.Z.O.O

FDA import alert and refusal historyLowicz, PolandFEI 3009929746

Recorded by FDA as ARGOS FORTUNA SP.Z.O.O

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Example subjectArgos Fortuna Sp.Z.O. added to Import Alert 16-129 (red list)

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As of October 26, 2026, Argos Fortuna Sp.Z.O.O is not on any FDA import alert in SupplierRadar's records; FDA refused 14 of its shipment lines between August 24, 2017 and August 1, 2023, most often for artificial coloring not declared (COLOR LBLG).

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

Current status

Import alerts
Not listed
Last import refusal
Apple, core fruit juices or concentrates · COLORLABEL
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Argos Fortuna Sp.Z.O.O

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

2023

  1. Import refusal
    Refused, 6 lines in one entry: Apple, core fruit juices or concentrates; Mango, juice, milk, creme, drink or nectar, sub/tropical fruit and 3 moreCOLORLABELCOLOR LBLGEntry 900-0170826-3Show 6 lines
    • Refused, Apple, core fruit juices or concentratesCOLORLABELEntry 900-0170826-3Source
    • Refused, Mango, juice, milk, creme, drink or nectar, sub/tropical fruitCOLORLABELEntry 900-0170826-3Source
    • Refused, Mango, juice, milk, creme, drink or nectar, sub/tropical fruitCOLOR LBLGEntry 900-0170826-3Source
    • Refused, Peach, juice, pit fruit juices or concentratesCOLORLABELEntry 900-0170826-3Source
    • Refused, Orange, citrus fruit juices or concentratesCOLORLABELEntry 900-0170826-3Source
    • Refused, Pineapple, juice, milk, creme, drink or nectar, sub/tropical fruitCOLORLABELEntry 900-0170826-3Source
    Source

2022

  1. Import refusal
    Refused, 5 lines in one entry: Beverage base not mentioned elsewhere, n.e.c.COLOR LBLGALLERGENEntry EH3-2174057-1Show 5 lines
    Source

2017

  1. Import refusal
    Refused, 3 lines in one entry: Vegetable (single ingredient not mentioned elsewhere) soupNEEDS FCENO PROCESSEntry 071-0218404-6Show 3 lines
    Source

2014

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

Refusal charges, in plain English

  • COLOR LBLG6 refused lines

    Artificial coloring not declared

    The product appeared to contain an artificial coloring without labeling that states that fact.

  • ALLERGEN5 refused lines

    Major food allergen not declared

    The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.

  • COLORLABEL5 refused lines

    Required information not prominent

    Information required on the label appeared not to be placed prominently enough, or in such terms, to be read and understood by an ordinary consumer.

  • NEEDS FCE3 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NO PROCESS3 refused lines

    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 Argos Fortuna Sp.Z.O.O

Is Argos Fortuna Sp.Z.O.O on an FDA import alert?
No listing for Argos Fortuna Sp.Z.O.O appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Poland page.
Has FDA refused shipments from Argos Fortuna Sp.Z.O.O?
Yes. FDA refused 14 shipment lines from Argos Fortuna Sp.Z.O.O between August 24, 2017 and August 1, 2023. The most recent, on August 1, 2023, was apple, core fruit juices or concentrates, charged as COLORLABEL (required information not prominent).
Why did FDA refuse Argos Fortuna Sp.Z.O.O's shipments?
The most frequent charges are COLOR LBLG (artificial coloring not declared, 6 lines) and ALLERGEN (major food allergen not declared, 5 lines).
When was Argos Fortuna Sp.Z.O.O last inspected by FDA?
FDA's most recent inspection of Argos Fortuna Sp.Z.O.O with a final classification is dated November 14, 2014 and was classified NAI (No Action Indicated).
What is Argos Fortuna Sp.Z.O.O's FEI number?
Argos Fortuna Sp.Z.O.O's FDA Establishment Identifier (FEI) is 3009929746.

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Example subjectArgos Fortuna Sp.Z.O. 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.