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Dr. Oetker Polska Sp. z o. o.

FDA import alert and refusal historyGdansk, PolandFEI 3004675587

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Example subjectDr. Oetker Polska Sp. z o. o added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dr. Oetker Polska Sp. z o. o. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 27, 2017, 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 Dr. Oetker Polska Sp. z o. o.

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

2017

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

2013

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

Questions about Dr. Oetker Polska Sp. z o. o.

Is Dr. Oetker Polska Sp. z o. o. on an FDA import alert?
No listing for Dr. Oetker Polska Sp. z o. o. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Poland page.
Has FDA refused shipments from Dr. Oetker Polska Sp. z o. o.?
No FDA import refusals for Dr. Oetker Polska Sp. z o. o. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Dr. Oetker Polska Sp. z o. o. last inspected by FDA?
FDA's most recent inspection of Dr. Oetker Polska Sp. z o. o. with a final classification is dated January 27, 2017 and was classified NAI (No Action Indicated).
What is Dr. Oetker Polska Sp. z o. o.'s FEI number?
Dr. Oetker Polska Sp. z o. o.'s FDA Establishment Identifier (FEI) is 3004675587.

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Example subjectDr. Oetker Polska Sp. z o. 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.