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Cerelia Belgium Bvba

FDA import alert and refusal historyVeurne, BelgiumFEI 3006337013

Recorded by FDA as CERELIA BELGIUM BVBA

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Example subjectCerelia Belgium Bvb added to Import Alert 16-129 (red list)

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As of October 26, 2026, Cerelia Belgium Bvba has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 12, 2023, 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 Cerelia Belgium Bvba

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

2023

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

2018

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

2013

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

Questions about Cerelia Belgium Bvba

Is Cerelia Belgium Bvba on an FDA import alert?
No listing for Cerelia Belgium Bvba 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 Cerelia Belgium Bvba?
No FDA import refusals for Cerelia Belgium Bvba appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Cerelia Belgium Bvba last inspected by FDA?
FDA's most recent inspection of Cerelia Belgium Bvba with a final classification is dated September 12, 2023 and was classified NAI (No Action Indicated).
What is Cerelia Belgium Bvba's FEI number?
Cerelia Belgium Bvba's FDA Establishment Identifier (FEI) is 3006337013.

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Example subjectCerelia Belgium Bvb 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.