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Tamek Gida Ve Konsantre Sanayii

⚠️ Moderate Risk

FEI: 3002954201 • Istanbul • TURKEY

FEI

FEI Number

3002954201

📍

Location

Istanbul

🇹🇷

Country

TURKEY
🏢

Address

No. 35 Ii.Ulus-Besiktas, , Istanbul, , Turkey

Moderate Risk

FDA Import Risk Assessment

35.5
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

5
Total Refusals
6
Unique Violations
3/24/2015
Latest Refusal
4/8/2002
Earliest Refusal

Score Breakdown

Violation Severity
66.3×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
3.9×10%
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

833×

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.

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

3211×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

Refusal History

DateProductViolationsDivision
3/24/2015
24HCT08PEPPER, HOT, DRIED OR PASTE
218LIST INGRE
321LACKS N/C
62NEEDS FCE
Baltimore District Office (BLT-DO)
10/6/2004
24TCP08CABBAGE (LEAF & STEM VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
10/6/2004
24FCP07PEPPER, SWEET (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
10/6/2004
24FCP01EGG PLANT (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
4/8/2002
24HCI50TOMATO, DRIED
249FILTHY
482NUTRIT LBL
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Tamek Gida Ve Konsantre Sanayii's FDA import refusal history?

Tamek Gida Ve Konsantre Sanayii (FEI: 3002954201) has 5 FDA import refusal record(s) in our database, spanning from 4/8/2002 to 3/24/2015.

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 Gida Ve Konsantre Sanayii's FEI number is 3002954201.

What types of violations has Tamek Gida Ve Konsantre Sanayii received?

Tamek Gida Ve Konsantre Sanayii has been cited for 6 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 Gida Ve Konsantre Sanayii come from?

All FDA import refusal data for Tamek Gida Ve Konsantre Sanayii 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.