Cheshni Gida AS
FDA import alert and refusal historyIstanbul, TurkeyFEI 3014441926
Recorded by FDA as CHESHNI GIDA AS
As of October 26, 2026, Cheshni Gida AS (Istanbul, Turkey) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for dried figs, published by FDA on March 15, 2019, and has 1 FDA import refusal 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
- Fig, dried or paste · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Cheshni Gida AS
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalRefused, Fig, dried or pastePESTICIDEEntry 8NR-0000696-7Source
- Import alert listingListed on Import Alert 99-08red listDried FigsSource
Refusal charges, in plain English
- PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Cheshni Gida AS
- Is Cheshni Gida AS on an FDA import alert?
- Yes. As of October 26, 2026, Cheshni Gida AS is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for dried figs; FDA published the listing on March 15, 2019.
- Has FDA refused shipments from Cheshni Gida AS?
- Yes. FDA refused 1 shipment line from Cheshni Gida AS on April 1, 2019. The most recent, on April 1, 2019, was fig, dried or paste, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Cheshni Gida AS's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Cheshni Gida AS's FEI number?
- Cheshni Gida AS's FDA Establishment Identifier (FEI) is 3014441926.
- Can shipments from Cheshni Gida AS still enter the U.S.?
- Shipments of dried figs from Cheshni Gida AS 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.