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TAMEK GRUP GIDA URETIM A.S.

⚠️ High Risk

FEI: 3024721183 • Bursa • TURKEY

FEI

FEI Number

3024721183

📍

Location

Bursa

🇹🇷

Country

TURKEY
🏢

Address

Kucukkaraagac Koyu Mevkii Karacabey, , Bursa, , Turkey

High Risk

FDA Import Risk Assessment

56.0
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

1
Total Refusals
1
Unique Violations
12/11/2025
Latest Refusal
12/11/2025
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
Refusal Volume
11.2×30%
Recency
98.4×20%
Frequency
10.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

831×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
12/11/2025
25ECT14TZAHP CHOY (CHINESE CANNED SWEET PICKLES MADE FROM MIXED VEGETABLES) (MIXED VEGETABLES)
83NO PROCESS
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is TAMEK GRUP GIDA URETIM A.S.'s FDA import refusal history?

TAMEK GRUP GIDA URETIM A.S. (FEI: 3024721183) has 1 FDA import refusal record(s) in our database, spanning from 12/11/2025 to 12/11/2025.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. TAMEK GRUP GIDA URETIM A.S.'s FEI number is 3024721183.

What types of violations has TAMEK GRUP GIDA URETIM A.S. received?

TAMEK GRUP GIDA URETIM A.S. has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about TAMEK GRUP GIDA URETIM A.S. come from?

All FDA import refusal data for TAMEK GRUP GIDA URETIM A.S. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.