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Marinus Enterprises

FDA import alert and refusal historyUrk, NetherlandsFEI 3009058206

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

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As of October 25, 2026, Marinus Enterprises is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between November 12, 2019 and December 19, 2019, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Flounder (arrowtooth, dab, fluke) · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Marinus Enterprises

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

2019

  1. Import refusal
    Refused, Flounder (arrowtooth, dab, fluke)FILTHYEntry AH5-0181441-4
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Flounder (arrowtooth, dab, fluke)FILTHYEntry AH5-0180836-6Show 2 lines
    • Refused, Flounder (arrowtooth, dab, fluke)FILTHYEntry AH5-0180836-6Source
    • Refused, Flounder (arrowtooth, dab, fluke)FILTHYEntry AH5-0180836-6Source
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • FILTHY3 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Marinus Enterprises

Is Marinus Enterprises on an FDA import alert?
No listing for Marinus Enterprises appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
Has FDA refused shipments from Marinus Enterprises?
Yes. FDA refused 3 shipment lines from Marinus Enterprises between November 12, 2019 and December 19, 2019. The most recent, on December 19, 2019, was flounder (arrowtooth, dab, fluke), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Marinus Enterprises's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
When was Marinus Enterprises last inspected by FDA?
FDA's most recent inspection of Marinus Enterprises with a final classification is dated December 5, 2018 and was classified VAI (Voluntary Action Indicated).
What is Marinus Enterprises's FEI number?
Marinus Enterprises's FDA Establishment Identifier (FEI) is 3009058206.

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Example subjectMarinus Enterprise 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.