Vitablend Nederland BV
FDA import alert and refusal historyWolvega, NetherlandsFEI 3004041082
As of October 25, 2026, Vitablend Nederland BV has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 4, 2023, 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 Vitablend Nederland BV
2 records, newest first. Each line links to the FDA page it came from.
Questions about Vitablend Nederland BV
- Is Vitablend Nederland BV on an FDA import alert?
- No listing for Vitablend Nederland BV appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
- Has FDA refused shipments from Vitablend Nederland BV?
- No FDA import refusals for Vitablend Nederland BV appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Vitablend Nederland BV last inspected by FDA?
- FDA's most recent inspection of Vitablend Nederland BV with a final classification is dated August 4, 2023 and was classified VAI (Voluntary Action Indicated).
- What is Vitablend Nederland BV's FEI number?
- Vitablend Nederland BV's FDA Establishment Identifier (FEI) is 3004041082.
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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.