Marenor Lysekil AB
FDA import alert and refusal historyLysekil, SwedenFEI 3010024291
As of October 26, 2026, Marenor Lysekil AB has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on April 25, 2023, was classified NAI (No 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 NAI (No Action Indicated)
Every FDA record for Marenor Lysekil AB
2 records, newest first. Each line links to the FDA page it came from.
Questions about Marenor Lysekil AB
- Is Marenor Lysekil AB on an FDA import alert?
- No listing for Marenor Lysekil AB appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Sweden page.
- Has FDA refused shipments from Marenor Lysekil AB?
- No FDA import refusals for Marenor Lysekil AB appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Marenor Lysekil AB last inspected by FDA?
- FDA's most recent inspection of Marenor Lysekil AB with a final classification is dated April 25, 2023 and was classified NAI (No Action Indicated).
- What is Marenor Lysekil AB's FEI number?
- Marenor Lysekil AB's FDA Establishment Identifier (FEI) is 3010024291.
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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.