Chr. Hansen A/S
FDA import alert and refusal historyHorsholm, DenmarkFEI 3002594255
As of October 26, 2026, Chr. Hansen A/S (Horsholm, Denmark) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for food related item, published by FDA on August 28, 2014, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Chr. Hansen A/S
3 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2016
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and EconSource
2014
- Import alert listingListed on Import Alert 45-02red listFood Related ItemSource
Questions about Chr. Hansen A/S
- Is Chr. Hansen A/S on an FDA import alert?
- Yes. As of October 26, 2026, Chr. Hansen A/S is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for food related item; FDA published the listing on August 28, 2014.
- Has FDA refused shipments from Chr. Hansen A/S?
- No FDA import refusals for Chr. Hansen A/S appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Chr. Hansen A/S last inspected by FDA?
- FDA's most recent inspection of Chr. Hansen A/S with a final classification is dated November 3, 2022 and was classified NAI (No Action Indicated).
- What is Chr. Hansen A/S's FEI number?
- Chr. Hansen A/S's FDA Establishment Identifier (FEI) is 3002594255.
- Can shipments from Chr. Hansen A/S still enter the U.S.?
- Shipments of food related item from Chr. Hansen A/S can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.