Novonesis A/S
FDA import alert and refusal historyRoskilde, DenmarkFEI 3004277341
As of October 25, 2026, Novonesis A/S has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on November 4, 2022, 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 Novonesis A/S
2 records, newest first. Each line links to the FDA page it came from.
Questions about Novonesis A/S
- Is Novonesis A/S on an FDA import alert?
- No listing for Novonesis A/S appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Denmark page.
- Has FDA refused shipments from Novonesis A/S?
- No FDA import refusals for Novonesis A/S appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Novonesis A/S last inspected by FDA?
- FDA's most recent inspection of Novonesis A/S with a final classification is dated November 4, 2022 and was classified VAI (Voluntary Action Indicated).
- What is Novonesis A/S's FEI number?
- Novonesis A/S's FDA Establishment Identifier (FEI) is 3004277341.
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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.