Jutrzenko Colian Sp. z o.o.
FDA import alert and refusal historyWykroty, PolandFEI 3007685061
As of October 26, 2026, Jutrzenko Colian Sp. z o.o. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 15, 2019, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Raisins, dried or paste · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Jutrzenko Colian Sp. z o.o.
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Jutrzenko Colian Sp. z o.o.
- Is Jutrzenko Colian Sp. z o.o. on an FDA import alert?
- No listing for Jutrzenko Colian 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 Jutrzenko Colian Sp. z o.o.?
- Yes. FDA refused 1 shipment line from Jutrzenko Colian Sp. z o.o. on March 15, 2019. The most recent, on March 15, 2019, was raisins, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Jutrzenko Colian Sp. z o.o.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was Jutrzenko Colian Sp. z o.o. last inspected by FDA?
- FDA's most recent inspection of Jutrzenko Colian Sp. z o.o. with a final classification is dated February 3, 2012 and was classified NAI (No Action Indicated).
- What is Jutrzenko Colian Sp. z o.o.'s FEI number?
- Jutrzenko Colian Sp. z o.o.'s FDA Establishment Identifier (FEI) is 3007685061.
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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.