Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti.
FDA import alert and refusal historyAntalya, TurkeyFEI 3003824720
As of October 26, 2026, Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti. (Antalya, 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 Mezo Ekolojik Urunler Gida Tarim Ithihr San 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, Whole (Spice); Cumin, Ground, Cracked (Spice)Source
Questions about Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti.
- Is Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti. on an FDA import alert?
- Yes. As of October 26, 2026, Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti. 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 Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti.?
- No FDA import refusals for Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti.'s FEI number?
- Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti.'s FDA Establishment Identifier (FEI) is 3003824720.
- Can shipments from Mezo Ekolojik Urunler Gida Tarim Ithihr San Ltd. Sti. still enter the U.S.?
- Shipments of cumin, whole (spice); cumin, ground, cracked (spice) from Mezo Ekolojik Urunler Gida Tarim Ithihr San 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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