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Greenyard Frozen Langemark NV

FDA import alert and refusal historyLangemark-Poelkapelle, BelgiumFEI 3009909948

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Example subjectGreenyard Frozen Langemark N added to Import Alert 16-129 (red list)

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As of October 26, 2026, Greenyard Frozen Langemark NV has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 24, 2024, was classified NAI (No Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Greenyard Frozen Langemark NV

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

2024

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

2019

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

Questions about Greenyard Frozen Langemark NV

Is Greenyard Frozen Langemark NV on an FDA import alert?
No listing for Greenyard Frozen Langemark NV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Belgium page.
Has FDA refused shipments from Greenyard Frozen Langemark NV?
No FDA import refusals for Greenyard Frozen Langemark NV appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Greenyard Frozen Langemark NV last inspected by FDA?
FDA's most recent inspection of Greenyard Frozen Langemark NV with a final classification is dated September 24, 2024 and was classified NAI (No Action Indicated).
What is Greenyard Frozen Langemark NV's FEI number?
Greenyard Frozen Langemark NV's FDA Establishment Identifier (FEI) is 3009909948.

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Example subjectGreenyard Frozen Langemark N 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.