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Biscuiterie Jules Destrooper

FDA import alert and refusal historyLo, BelgiumFEI 3005018454

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Example subjectBiscuiterie Jules Destroope added to Import Alert 16-129 (red list)

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As of October 26, 2026, Biscuiterie Jules Destrooper has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 8, 2019, 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 Biscuiterie Jules Destrooper

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

2019

  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)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Biscuiterie Jules Destrooper

Is Biscuiterie Jules Destrooper on an FDA import alert?
No listing for Biscuiterie Jules Destrooper 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 Biscuiterie Jules Destrooper?
No FDA import refusals for Biscuiterie Jules Destrooper appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Biscuiterie Jules Destrooper last inspected by FDA?
FDA's most recent inspection of Biscuiterie Jules Destrooper with a final classification is dated January 8, 2019 and was classified NAI (No Action Indicated).
What is Biscuiterie Jules Destrooper's FEI number?
Biscuiterie Jules Destrooper's FDA Establishment Identifier (FEI) is 3005018454.

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Example subjectBiscuiterie Jules Destroope 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.