Vitux AS
FDA import alert and refusal historyAndenes, NorwayFEI 3009858805
As of October 26, 2026, Vitux AS has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 15, 2024, 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 Vitux AS
2 records, newest first. Each line links to the FDA page it came from.
Questions about Vitux AS
- Is Vitux AS on an FDA import alert?
- No listing for Vitux AS appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Norway page.
- Has FDA refused shipments from Vitux AS?
- No FDA import refusals for Vitux AS appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Vitux AS last inspected by FDA?
- FDA's most recent inspection of Vitux AS with a final classification is dated August 15, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Vitux AS's FEI number?
- Vitux AS's FDA Establishment Identifier (FEI) is 3009858805.
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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.