Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti.
FDA import alert and refusal historyIzmir, TurkeyFEI 3003492691
As of October 26, 2026, Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti. (Izmir, Turkey) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for 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 Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listCumin, Ground, Cracked (Spice)Source
Questions about Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti.
- Is Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti. on an FDA import alert?
- Yes. As of October 26, 2026, Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for cumin, ground, cracked (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti.?
- No FDA import refusals for Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti.'s FEI number?
- Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti.'s FDA Establishment Identifier (FEI) is 3003492691.
- Can shipments from Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti. still enter the U.S.?
- Shipments of cumin, ground, cracked (spice) from Meba Tarim Urunleri Sanayi Ve Ticaret Ltd Sti. 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.