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TAMEK GIDA VE KONSANTRE SAN. VE TIC. A.S.

⚠️ Moderate Risk

FEI: 3006424615 • Salihli, Manisa • TURKEY

FEI

FEI Number

3006424615

📍

Location

Salihli, Manisa

🇹🇷

Country

TURKEY
🏢

Address

Bezirganli Mah., Gedizler Cad. No 71 Bezirganli Mevkii, Salihli, Manisa, Turkey

Moderate Risk

FDA Import Risk Assessment

41.2
LowModerateHighCritical

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

Statistics

11
Total Refusals
10
Unique Violations
3/20/2012
Latest Refusal
5/13/2010
Earliest Refusal

Score Breakdown

Violation Severity
58.1×40%
Refusal Volume
40.0×30%
Recency
0.0×20%
Frequency
59.3×10%
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

839×

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.

4825×

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.

623×

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).

4732×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

3282×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

3242×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

33001×

ALLERGEN

the label fails to declare all major food allergens present in the product, as required by section 403(w)(1).

3201×

LACKS FIRM

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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

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.

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.

Refusal History

DateProductViolationsDivision
3/20/2012
24FEE01EGG PLANT (FRUIT USED AS VEGETABLE)
482NUTRIT LBL
New York District Office (NYK-DO)
6/6/2011
24FET01EGG PLANT (FRUIT USED AS VEGETABLE)
324NO ENGLISH
328USUAL NAME
473LABELING
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
6/6/2011
27AGT02MAYONNAISE
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
3300ALLERGEN
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
4/20/2011
24FCE07PEPPER, SWEET (FRUIT USED AS VEGETABLE)
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
4/20/2011
24FCE01EGG PLANT (FRUIT USED AS VEGETABLE)
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
New York District Office (NYK-DO)
5/13/2010
24HEE07PEPPER, SWEET, DRIED OR PASTE
83NO PROCESS
New York District Office (NYK-DO)
5/13/2010
24FCT01EGG PLANT (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
5/13/2010
24FCT01EGG PLANT (FRUIT USED AS VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)
5/13/2010
24AEE06GARBANZO BEAN
83NO PROCESS
New York District Office (NYK-DO)
5/13/2010
24AEE07KIDNEY BEAN
83NO PROCESS
New York District Office (NYK-DO)
5/13/2010
24AEE99BEANS, CORN, AND PEA, N.E.C. (VEGETABLE)
83NO PROCESS
New York District Office (NYK-DO)

Frequently Asked Questions

What is TAMEK GIDA VE KONSANTRE SAN. VE TIC. A.S.'s FDA import refusal history?

TAMEK GIDA VE KONSANTRE SAN. VE TIC. A.S. (FEI: 3006424615) has 11 FDA import refusal record(s) in our database, spanning from 5/13/2010 to 3/20/2012.

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 SAN. VE TIC. A.S.'s FEI number is 3006424615.

What types of violations has TAMEK GIDA VE KONSANTRE SAN. VE TIC. A.S. received?

TAMEK GIDA VE KONSANTRE SAN. VE TIC. A.S. has been cited for 10 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 SAN. VE TIC. A.S. come from?

All FDA import refusal data for TAMEK GIDA VE KONSANTRE SAN. VE TIC. 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.