Ardo N.V.
FDA import alert and refusal historyArdooie, BelgiumFEI 3004030235
As of October 26, 2026, Ardo N.V. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 5, 2013, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)
Every FDA record for Ardo N.V.
3 records, newest first. Each line links to the FDA page it came from.
2019
- RecallRecall (Class II), Trader Joe s Vegetable Melange In Seasoned Butter Sauce Packed in 16 ounce plastic packages retail packaging Bar code: 0033 7038Product label lists butter as an ingredient but does not declare milk.Source
- RecallRecall (Class II), Trader Joe s Fire Roasted Vegetables With Balsamic Butter Sauce Packed in 16 ounce plastic packages retail packaging Bar code: 0077 5175Product label lists butter as an ingredient but does not declare milk.Source
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Ardo N.V.
- Is Ardo N.V. on an FDA import alert?
- No listing for Ardo N.V. 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 Ardo N.V.?
- No FDA import refusals for Ardo N.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Ardo N.V. last inspected by FDA?
- FDA's most recent inspection of Ardo N.V. with a final classification is dated September 5, 2013 and was classified VAI (Voluntary Action Indicated).
- What is Ardo N.V.'s FEI number?
- Ardo N.V.'s FDA Establishment Identifier (FEI) is 3004030235.
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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.