Donia d.o.o.
FDA import alert and refusal historyPrilep, North MacedoniaFEI 3010143348
As of October 25, 2026, Donia d.o.o. (Prilep, North Macedonia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for traditional turkish delight, published by FDA on July 13, 2011, 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 VAI (Voluntary Action Indicated)
Every FDA record for Donia d.o.o.
2 records, newest first. Each line links to the FDA page it came from.
2015
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 45-02red listTraditional Turkish DelightSource
Questions about Donia d.o.o.
- Is Donia d.o.o. on an FDA import alert?
- Yes. As of October 25, 2026, Donia d.o.o. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for traditional turkish delight; FDA published the listing on July 13, 2011.
- Has FDA refused shipments from Donia d.o.o.?
- No FDA import refusals for Donia d.o.o. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Donia d.o.o. last inspected by FDA?
- FDA's most recent inspection of Donia d.o.o. with a final classification is dated February 24, 2015 and was classified VAI (Voluntary Action Indicated).
- What is Donia d.o.o.'s FEI number?
- Donia d.o.o.'s FDA Establishment Identifier (FEI) is 3010143348.
- Can shipments from Donia d.o.o. still enter the U.S.?
- Shipments of traditional turkish delight from Donia d.o.o. 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.