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H. Van Wijnen B.V.

FDA import alert and refusal historyKrimpen Aan Den Ijssel, NetherlandsFEI 3009200230

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Example subjectH. Van Wijnen B.V added to Import Alert 16-129 (red list)

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As of October 25, 2026, H. Van Wijnen B.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on December 28, 2016, 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
Salmon (humpback, silver, king, sockeye, etc.), cold smoked, fish · LISTERIA
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for H. Van Wijnen B.V.

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

2018

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2016

  1. Import refusal
    Refused, Salmon (humpback, silver, king, sockeye, etc.), cold smoked, fishLISTERIAEntry 594-0276280-7
    Source
  2. Import refusal
    Refused, Salmon (humpback, silver, king, sockeye, etc.), cold smoked, fishLISTERIAEntry 594-0276279-9
    Source

Refusal charges, in plain English

  • LISTERIA2 refused lines

    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 H. Van Wijnen B.V.

Is H. Van Wijnen B.V. on an FDA import alert?
No listing for H. Van Wijnen B.V. 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 H. Van Wijnen B.V.?
Yes. FDA refused 2 shipment lines from H. Van Wijnen B.V. on December 28, 2016. The most recent, on December 28, 2016, was salmon (humpback, silver, king, sockeye, etc.), cold smoked, fish, charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse H. Van Wijnen B.V.'s shipments?
The most frequent charge is LISTERIA (listeria monocytogenes, 2 lines).
When was H. Van Wijnen B.V. last inspected by FDA?
FDA's most recent inspection of H. Van Wijnen B.V. with a final classification is dated September 4, 2018 and was classified NAI (No Action Indicated).
What is H. Van Wijnen B.V.'s FEI number?
H. Van Wijnen B.V.'s FDA Establishment Identifier (FEI) is 3009200230.

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Example subjectH. Van Wijnen B.V 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.