Mieszko S.A. (Facility 1)
FDA import alert and refusal historyRaciborz, PolandFEI 3009941851
As of October 26, 2026, Mieszko S.A. (Facility 1) (Raciborz, Poland) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for candy without chocolate n.e.c., published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Mieszko S.A. (Facility 1)
2 records, newest first. Each line links to the FDA page it came from.
2014
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 45-02red listCandy Without Chocolate N.E.C.Source
Questions about Mieszko S.A. (Facility 1)
- Is Mieszko S.A. (Facility 1) on an FDA import alert?
- Yes. As of October 26, 2026, Mieszko S.A. (Facility 1) is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for candy without chocolate n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Mieszko S.A. (Facility 1)?
- No FDA import refusals for Mieszko S.A. (Facility 1) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Mieszko S.A. (Facility 1) last inspected by FDA?
- FDA's most recent inspection of Mieszko S.A. (Facility 1) with a final classification is dated November 21, 2014 and was classified NAI (No Action Indicated).
- What is Mieszko S.A. (Facility 1)'s FEI number?
- Mieszko S.A. (Facility 1)'s FDA Establishment Identifier (FEI) is 3009941851.
- Can shipments from Mieszko S.A. (Facility 1) still enter the U.S.?
- Shipments of candy without chocolate n.e.c. from Mieszko S.A. (Facility 1) can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.