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Przetworstwo Spozywcze s.c.

FDA import alert and refusal historyLegionowo, PolandFEI 3004275916

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Example subjectPrzetworstwo Spozywcze s.c added to Import Alert 16-129 (red list)

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As of October 26, 2026, Przetworstwo Spozywcze s.c. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 5, 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 Przetworstwo Spozywcze s.c.

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

2013

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

Questions about Przetworstwo Spozywcze s.c.

Is Przetworstwo Spozywcze s.c. on an FDA import alert?
No listing for Przetworstwo Spozywcze s.c. 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 Przetworstwo Spozywcze s.c.?
No FDA import refusals for Przetworstwo Spozywcze s.c. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Przetworstwo Spozywcze s.c. last inspected by FDA?
FDA's most recent inspection of Przetworstwo Spozywcze s.c. with a final classification is dated September 5, 2018 and was classified VAI (Voluntary Action Indicated).
What is Przetworstwo Spozywcze s.c.'s FEI number?
Przetworstwo Spozywcze s.c.'s FDA Establishment Identifier (FEI) is 3004275916.

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Example subjectPrzetworstwo Spozywcze s.c 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.