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Kaeserei H Birkenstock GmbH

FDA import alert and refusal historyHuttenberg, GermanyFEI 3003013783

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Example subjectKaeserei H Birkenstock Gmb added to Import Alert 16-129 (red list)

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As of October 26, 2026, Kaeserei H Birkenstock GmbH has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on July 12, 2022, 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 Kaeserei H Birkenstock GmbH

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

2022

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

2013

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Questions about Kaeserei H Birkenstock GmbH

Is Kaeserei H Birkenstock GmbH on an FDA import alert?
No listing for Kaeserei H Birkenstock GmbH appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
Has FDA refused shipments from Kaeserei H Birkenstock GmbH?
No FDA import refusals for Kaeserei H Birkenstock GmbH appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Kaeserei H Birkenstock GmbH last inspected by FDA?
FDA's most recent inspection of Kaeserei H Birkenstock GmbH with a final classification is dated July 12, 2022 and was classified VAI (Voluntary Action Indicated).
What is Kaeserei H Birkenstock GmbH's FEI number?
Kaeserei H Birkenstock GmbH's FDA Establishment Identifier (FEI) is 3003013783.

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Example subjectKaeserei H Birkenstock Gmb 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.