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Greenyard Prepared Belgium NV

FDA import alert and refusal historyBree, BelgiumFEI 3004301156

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Example subjectGreenyard Prepared Belgium N added to Import Alert 16-129 (red list)

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As of October 26, 2026, Greenyard Prepared Belgium NV has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 7, 2016, 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 Prepared Belgium NV

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

2016

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

2013

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

Questions about Greenyard Prepared Belgium NV

Is Greenyard Prepared Belgium NV on an FDA import alert?
No listing for Greenyard Prepared Belgium 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 Prepared Belgium NV?
No FDA import refusals for Greenyard Prepared Belgium NV appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Greenyard Prepared Belgium NV last inspected by FDA?
FDA's most recent inspection of Greenyard Prepared Belgium NV with a final classification is dated December 7, 2016 and was classified NAI (No Action Indicated).
What is Greenyard Prepared Belgium NV's FEI number?
Greenyard Prepared Belgium NV's FDA Establishment Identifier (FEI) is 3004301156.

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Example subjectGreenyard Prepared Belgium 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.