Belova Tarim Orman Urunleri San.ve Tic. A.S.
FDA import alert and refusal historyIzmir, TurkeyFEI 2000003874
As of October 27, 2026, Belova Tarim Orman Urunleri San.ve Tic. A.S. (Izmir, Turkey) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for cumin, whole (spice); cumin, ground, cracked (spice), published by FDA on September 16, 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Belova Tarim Orman Urunleri San.ve Tic. A.S.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listCumin, Whole (Spice); Cumin, Ground, Cracked (Spice)Source
Questions about Belova Tarim Orman Urunleri San.ve Tic. A.S.
- Is Belova Tarim Orman Urunleri San.ve Tic. A.S. on an FDA import alert?
- Yes. As of October 27, 2026, Belova Tarim Orman Urunleri San.ve Tic. A.S. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for cumin, whole (spice); cumin, ground, cracked (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Belova Tarim Orman Urunleri San.ve Tic. A.S.?
- No FDA import refusals for Belova Tarim Orman Urunleri San.ve Tic. A.S. appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Belova Tarim Orman Urunleri San.ve Tic. A.S.'s FEI number?
- Belova Tarim Orman Urunleri San.ve Tic. A.S.'s FDA Establishment Identifier (FEI) is 2000003874.
- Can shipments from Belova Tarim Orman Urunleri San.ve Tic. A.S. still enter the U.S.?
- Shipments of cumin, whole (spice); cumin, ground, cracked (spice) from Belova Tarim Orman Urunleri San.ve Tic. A.S. can be detained without physical examination under Import Alert 99-19; 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.