Brodrene Sperre
FDA import alert and refusal historyEllingsoy, NorwayFEI 3011137773
As of October 25, 2026, Brodrene Sperre has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 17, 2016, 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 Brodrene Sperre
2 records, newest first. Each line links to the FDA page it came from.
Questions about Brodrene Sperre
- Is Brodrene Sperre on an FDA import alert?
- No listing for Brodrene Sperre appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Norway page.
- Has FDA refused shipments from Brodrene Sperre?
- No FDA import refusals for Brodrene Sperre appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Brodrene Sperre last inspected by FDA?
- FDA's most recent inspection of Brodrene Sperre with a final classification is dated June 17, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Brodrene Sperre's FEI number?
- Brodrene Sperre's FDA Establishment Identifier (FEI) is 3011137773.
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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.