Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin
FDA import alert and refusal history35090 Camidibi-Izmir, TurkeyFEI 3002668461
As of October 27, 2026, Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin (35090 Camidibi-Izmir, Turkey) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for cherries;sour; dried, 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 Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listcherries;sour; driedSource
Questions about Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin
- Is Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin on an FDA import alert?
- Yes. As of October 27, 2026, Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for cherries;sour; dried; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin?
- No FDA import refusals for Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin's FEI number?
- Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin's FDA Establishment Identifier (FEI) is 3002668461.
- Can shipments from Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin still enter the U.S.?
- Shipments of cherries;sour; dried from Malatya Kayisi Pazari Malatya Apricot Market Adnan Gultekin 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.