Tamek Grup Gida Uretim A.S.
FDA import alert and refusal historyBursa, TurkeyFEI 3024721183
Recorded by FDA as TAMEK GRUP GIDA URETIM A.S.
As of October 26, 2026, Tamek Grup Gida Uretim A.S. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 11, 2025, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tzahp choy (chinese canned sweet pickles made from mixed vegetables) (mixed vegetables) · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Tamek Grup Gida Uretim A.S.
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Tzahp choy (chinese canned sweet pickles made from mixed vegetables) (mixed vegetables)NO PROCESSEntry 523-1452262-5Source
Refusal charges, in plain English
- NO PROCESS1 refused line
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Tamek Grup Gida Uretim A.S.
- Is Tamek Grup Gida Uretim A.S. on an FDA import alert?
- No listing for Tamek Grup Gida Uretim A.S. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Turkey page.
- Has FDA refused shipments from Tamek Grup Gida Uretim A.S.?
- Yes. FDA refused 1 shipment line from Tamek Grup Gida Uretim A.S. on December 11, 2025. The most recent, on December 11, 2025, was tzahp choy (chinese canned sweet pickles made from mixed vegetables) (mixed vegetables), charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Tamek Grup Gida Uretim A.S.'s shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
- What is Tamek Grup Gida Uretim A.S.'s FEI number?
- Tamek Grup Gida Uretim A.S.'s FDA Establishment Identifier (FEI) is 3024721183.
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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.