Arla Foods A.m.b.a. Hoegelund Mejeri
FDA import alert and refusal historyVojens, DenmarkFEI 3004280208
As of October 27, 2026, Arla Foods A.m.b.a. Hoegelund Mejeri has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 1, 2024, 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 Arla Foods A.m.b.a. Hoegelund Mejeri
3 records, newest first. Each line links to the FDA page it came from.
2024
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2016
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2010
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Questions about Arla Foods A.m.b.a. Hoegelund Mejeri
- Is Arla Foods A.m.b.a. Hoegelund Mejeri on an FDA import alert?
- No listing for Arla Foods A.m.b.a. Hoegelund Mejeri appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Denmark page.
- Has FDA refused shipments from Arla Foods A.m.b.a. Hoegelund Mejeri?
- No FDA import refusals for Arla Foods A.m.b.a. Hoegelund Mejeri appear in FDA's refusal data since October 2016, as of October 27, 2026.
- When was Arla Foods A.m.b.a. Hoegelund Mejeri last inspected by FDA?
- FDA's most recent inspection of Arla Foods A.m.b.a. Hoegelund Mejeri with a final classification is dated March 1, 2024 and was classified NAI (No Action Indicated).
- What is Arla Foods A.m.b.a. Hoegelund Mejeri's FEI number?
- Arla Foods A.m.b.a. Hoegelund Mejeri's FDA Establishment Identifier (FEI) is 3004280208.
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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.