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Austria Juice Poland Sp. z o.o

FDA import alert and refusal historyKholm, PolandFEI 3004138703

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Example subjectAustria Juice Poland Sp. z o. added to Import Alert 16-129 (red list)

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As of October 27, 2026, Austria Juice Poland Sp. z o.o has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 17, 2018, 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 Austria Juice Poland Sp. z o.o

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

2018

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

2011

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

Questions about Austria Juice Poland Sp. z o.o

Is Austria Juice Poland Sp. z o.o on an FDA import alert?
No listing for Austria Juice Poland Sp. z o.o appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Poland page.
Has FDA refused shipments from Austria Juice Poland Sp. z o.o?
No FDA import refusals for Austria Juice Poland Sp. z o.o appear in FDA's refusal data since October 2016, as of October 27, 2026.
When was Austria Juice Poland Sp. z o.o last inspected by FDA?
FDA's most recent inspection of Austria Juice Poland Sp. z o.o with a final classification is dated September 17, 2018 and was classified VAI (Voluntary Action Indicated).
What is Austria Juice Poland Sp. z o.o's FEI number?
Austria Juice Poland Sp. z o.o's FDA Establishment Identifier (FEI) is 3004138703.

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Example subjectAustria Juice Poland Sp. z o. 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.