Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi
FDA import alert and refusal historyLapseki, TurkeyFEI 3007150950
As of October 27, 2026, Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi (Lapseki, Turkey) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for cherry fruit (pit fruit), 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listCherry Fruit (Pit Fruit)Source
Questions about Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi
- Is Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi on an FDA import alert?
- Yes. As of October 27, 2026, Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for cherry fruit (pit fruit); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi?
- No FDA import refusals for Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi's FEI number?
- Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi's FDA Establishment Identifier (FEI) is 3007150950.
- Can shipments from Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi still enter the U.S.?
- Shipments of cherry fruit (pit fruit) from Ulubay Soguk Depo Isletmeciligi ve Ticaret Limited Sirketi can be detained without physical examination under Import Alert 99-08; 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.