Klas dd Sarajevo
FDA import alert and refusal historySarajevo, Bosnia and HerzegovinaFEI 3005088268
As of October 25, 2026, Klas dd Sarajevo (Sarajevo, Bosnia and Herzegovina) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for homemade baklava; hurmasica pastry, published by FDA on July 17, 2025, 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 99-39 · 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 Klas dd Sarajevo
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 99-39red listHomemade Baklava; Hurmasica PastrySource
2024
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Klas dd Sarajevo
- Is Klas dd Sarajevo on an FDA import alert?
- Yes. As of October 25, 2026, Klas dd Sarajevo is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for homemade baklava; hurmasica pastry; FDA published the listing on July 17, 2025.
- Has FDA refused shipments from Klas dd Sarajevo?
- No FDA import refusals for Klas dd Sarajevo appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Klas dd Sarajevo last inspected by FDA?
- FDA's most recent inspection of Klas dd Sarajevo with a final classification is dated February 29, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Klas dd Sarajevo's FEI number?
- Klas dd Sarajevo's FDA Establishment Identifier (FEI) is 3005088268.
- Can shipments from Klas dd Sarajevo still enter the U.S.?
- Shipments of homemade baklava; hurmasica pastry from Klas dd Sarajevo can be detained without physical examination under Import Alert 99-39; 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.