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Fromagers en Bourgogne

FDA import alert and refusal historyVerdun Sur le Doubs, FranceFEI 3004284210

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Example subjectFromagers en Bourgogn added to Import Alert 16-129 (red list)

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As of October 25, 2026, Fromagers en Bourgogne is on the green list of FDA Import Alert 12-03, which exempts its listed products from detention without physical examination under that alert, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Fromagers en Bourgogne

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

2011

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

2009

  1. Import alert listing
    Listed on Import Alert 12-03green listAll soft and soft-ripened cheeses made from cows (vache) milk
    Source

Questions about Fromagers en Bourgogne

Is Fromagers en Bourgogne on an FDA import alert?
Yes. As of October 25, 2026, Fromagers en Bourgogne is on the green list of FDA Import Alert 12-03, “Soft and soft-ripened cheese from France”, for all soft and soft-ripened cheeses made from cows (vache) milk; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Fromagers en Bourgogne?
No FDA import refusals for Fromagers en Bourgogne appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Fromagers en Bourgogne last inspected by FDA?
FDA's most recent inspection of Fromagers en Bourgogne with a final classification is dated September 27, 2011 and was classified NAI (No Action Indicated).
What is Fromagers en Bourgogne's FEI number?
Fromagers en Bourgogne's FDA Establishment Identifier (FEI) is 3004284210.

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Example subjectFromagers en Bourgogn 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.