Ardo Violaines SA
FDA import alert and refusal historyViolaines, FranceFEI 3004270851
As of October 26, 2026, Ardo Violaines SA (Violaines, France) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for brussels sprouts, published by FDA on February 20, 2013, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Ardo Violaines SA
2 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2013
- Import alert listingListed on Import Alert 99-08red listBrussels SproutsSource
Questions about Ardo Violaines SA
- Is Ardo Violaines SA on an FDA import alert?
- Yes. As of October 26, 2026, Ardo Violaines SA is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for brussels sprouts; FDA published the listing on February 20, 2013.
- Has FDA refused shipments from Ardo Violaines SA?
- No FDA import refusals for Ardo Violaines SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Ardo Violaines SA last inspected by FDA?
- FDA's most recent inspection of Ardo Violaines SA with a final classification is dated June 21, 2018 and was classified NAI (No Action Indicated).
- What is Ardo Violaines SA's FEI number?
- Ardo Violaines SA's FDA Establishment Identifier (FEI) is 3004270851.
- Can shipments from Ardo Violaines SA still enter the U.S.?
- Shipments of brussels sprouts from Ardo Violaines SA can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.