SupplierRadar

Agustson A/S

FDA import alert and refusal historyVejle, DenmarkFEI 2000022606

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Example subjectAgustson A/ added to Import Alert 16-129 (red list)

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As of October 26, 2026, Agustson A/S has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 5, 2024, was classified OAI (Official 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
Acidified Foods/Emergency Permit Control/Adulterated
Last inspection
Classified OAI (Official Action Indicated)

Every FDA record for Agustson A/S

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

2024

  1. Warning letter
    Warning letter issuedAcidified Foods/Emergency Permit Control/Adulterated
    Source
  2. Inspection
    Inspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about Agustson A/S

Is Agustson A/S on an FDA import alert?
No listing for Agustson A/S appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Denmark page.
Has FDA refused shipments from Agustson A/S?
No FDA import refusals for Agustson A/S appear in FDA's refusal data since October 2016, as of October 26, 2026.
Has Agustson A/S received an FDA warning letter?
Yes. FDA issued a warning letter to Agustson A/S on August 13, 2024 (Acidified Foods/Emergency Permit Control/Adulterated).
When was Agustson A/S last inspected by FDA?
FDA's most recent inspection of Agustson A/S with a final classification is dated March 5, 2024 and was classified OAI (Official Action Indicated).
What is Agustson A/S's FEI number?
Agustson A/S's FDA Establishment Identifier (FEI) is 2000022606.

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Example subjectAgustson A/ 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.