An Gida Uretim Ve Pazarlama A.S.
FDA import alert and refusal historyBozdogan, TurkeyFEI 3004265898
As of October 26, 2026, An Gida Uretim Ve Pazarlama A.S. (Bozdogan, Turkey) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for grape leaves, published by FDA on May 6, 2014, is also listed on Import Alert 45-02 (red list) and Import Alert 99-19 (red list), and has 14 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Last import refusal
- Mint, whole (spice) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for An Gida Uretim Ve Pazarlama A.S.
18 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Mint, whole (spice)SALMONELLAEntry F23-9329289-1Source
- Import refusalRefused, Leaf & stem vegetables, n.e.c.PESTICIDEEntry DP4-3909108-4Source
2023
- Import refusalRefused, Candy specialties, n.e.c. (without chocolate)UNSAFE COLEntry F23-9289649-4Source
2022
- Import refusalSource
Refused, 2 lines in one entry: Cabbage (leaf & stem vegetable)NUTRIT LBLLABELINGEntry F23-9272313-6Show 2 linesHide lines
- Refused, Cabbage (leaf & stem vegetable)NUTRIT LBLEntry F23-9272313-6Source
- Refused, Cabbage (leaf & stem vegetable)LABELINGNUTRIT LBLEntry F23-9272313-6Source
2021
- Import refusalRefused, Mint, whole (spice)SALMONELLAEntry J89-0135468-0Source
2020
- Import refusalRefused, Mint, whole (spice)SALMONELLAEntry J89-0135322-9Source
- Import refusalRefused, Mint, whole (spice)SALMONELLAEntry J89-0135485-4Source
- Import refusalRefused, Mint, whole (spice)SALMONELLAEntry J89-0135410-2Source
2019
2018
2017
2014
- Import alert listingListed on Import Alert 99-08red listGrape LeavesSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 45-02red listAkide Sekeri ( Hard Candy); Akide Sekeri (candy)Source
Show 1 earlier record (2009)Hide earlier records
2009
- Import alert listingListed on Import Alert 99-19red listMint; dried; MahlebSource
Refusal charges, in plain English
- PESTICIDE6 refused lines
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.
- SALMONELLA5 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about An Gida Uretim Ve Pazarlama A.S.
- Is An Gida Uretim Ve Pazarlama A.S. on an FDA import alert?
- Yes. As of October 26, 2026, An Gida Uretim Ve Pazarlama A.S. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for grape leaves; FDA published the listing on May 6, 2014.
- Has FDA refused shipments from An Gida Uretim Ve Pazarlama A.S.?
- Yes. FDA refused 14 shipment lines from An Gida Uretim Ve Pazarlama A.S. between July 27, 2017 and May 21, 2025. The most recent, on May 21, 2025, was mint, whole (spice), charged as SALMONELLA (salmonella).
- Why did FDA refuse An Gida Uretim Ve Pazarlama A.S.'s shipments?
- The most frequent charges are PESTICIDE (pesticide chemical residue, 6 lines) and SALMONELLA (salmonella, 5 lines).
- When was An Gida Uretim Ve Pazarlama A.S. last inspected by FDA?
- FDA's most recent inspection of An Gida Uretim Ve Pazarlama A.S. with a final classification is dated April 6, 2012 and was classified VAI (Voluntary Action Indicated).
- What is An Gida Uretim Ve Pazarlama A.S.'s FEI number?
- An Gida Uretim Ve Pazarlama A.S.'s FDA Establishment Identifier (FEI) is 3004265898.
- Can shipments from An Gida Uretim Ve Pazarlama A.S. still enter the U.S.?
- Shipments of grape leaves from An Gida Uretim Ve Pazarlama A.S. 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.