DAWTONA Sp.zo.o
FDA import alert and refusal historyLeszno, PolandFEI 3012652962
As of October 26, 2026, DAWTONA Sp.zo.o (Leszno, Poland) is on the red list of FDA Import Alert 99-38 (Low-acid canned/acidified foods: inadequate process control) for lacf green peas in brine, published by FDA on January 16, 2026, 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 99-38 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for DAWTONA Sp.zo.o
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-38red listLACF Green Peas in BrineSource
2025
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about DAWTONA Sp.zo.o
- Is DAWTONA Sp.zo.o on an FDA import alert?
- Yes. As of October 26, 2026, DAWTONA Sp.zo.o is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for lacf green peas in brine; FDA published the listing on January 16, 2026.
- Has FDA refused shipments from DAWTONA Sp.zo.o?
- No FDA import refusals for DAWTONA Sp.zo.o appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was DAWTONA Sp.zo.o last inspected by FDA?
- FDA's most recent inspection of DAWTONA Sp.zo.o with a final classification is dated June 27, 2025 and was classified OAI (Official Action Indicated).
- What is DAWTONA Sp.zo.o's FEI number?
- DAWTONA Sp.zo.o's FDA Establishment Identifier (FEI) is 3012652962.
- Can shipments from DAWTONA Sp.zo.o still enter the U.S.?
- Shipments of lacf green peas in brine from DAWTONA Sp.zo.o can be detained without physical examination under Import Alert 99-38; 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.