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Lantmannen Cerealia Laholm

FDA import alert and refusal historyLaholm, SwedenFEI 3010167205

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Example subjectLantmannen Cerealia Lahol added to Import Alert 16-129 (red list)

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As of October 26, 2026, Lantmannen Cerealia Laholm has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 9, 2019, 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 Lantmannen Cerealia Laholm

2 records, newest first. Each line links to the FDA page it came from.

2019

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2014

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Lantmannen Cerealia Laholm

Is Lantmannen Cerealia Laholm on an FDA import alert?
No listing for Lantmannen Cerealia Laholm 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 Lantmannen Cerealia Laholm?
No FDA import refusals for Lantmannen Cerealia Laholm appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Lantmannen Cerealia Laholm last inspected by FDA?
FDA's most recent inspection of Lantmannen Cerealia Laholm with a final classification is dated May 9, 2019 and was classified VAI (Voluntary Action Indicated).
What is Lantmannen Cerealia Laholm's FEI number?
Lantmannen Cerealia Laholm's FDA Establishment Identifier (FEI) is 3010167205.

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Example subjectLantmannen Cerealia Lahol added to Import Alert 16-129 (red list)

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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.