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Odem Gida Petrol Ve Orman Urunle

⚠️ Moderate Risk

FEI: 3008733114 • Konya • TURKEY

FEI

FEI Number

3008733114

📍

Location

Konya

🇹🇷

Country

TURKEY
🏢

Address

Musalla Baglari Mah Eski No 2e, , Konya, , Turkey

Moderate Risk

FDA Import Risk Assessment

36.9
LowModerateHighCritical

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

Statistics

8
Total Refusals
9
Unique Violations
5/23/2013
Latest Refusal
6/5/2012
Earliest Refusal

Score Breakdown

Violation Severity
45.6×40%
Refusal Volume
35.3×30%
Recency
0.0×20%
Frequency
80.0×10%
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

3244×

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)).

2653×

SUBSTITUTE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears that a substance has been substituted wholly or in part for one or more of the article's ingredients.

4823×

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.

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.

3281×

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.

4731×

LABELING

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

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.

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.

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.

Refusal History

DateProductViolationsDivision
5/23/2013
03TDT25PASTRY (OTHER THAN FRUIT OR JELLY FILLED) DOUGH OR BATTER WITHOUT CUSTARD OR CREAM FILLING
324NO ENGLISH
482NUTRIT LBL
New York District Office (NYK-DO)
5/23/2013
36DCT99IMITATION SYRUPS, MOLASSES AND HONEY, N.E.C.
324NO ENGLISH
New York District Office (NYK-DO)
5/23/2013
21GGH17SLOE (PIT FRUIT)
324NO ENGLISH
New York District Office (NYK-DO)
5/23/2013
24BGH99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE)
218LIST INGRE
320LACKS FIRM
321LACKS N/C
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)
7/31/2012
36CCD04HONEY
265SUBSTITUTE
New York District Office (NYK-DO)
7/31/2012
36CCD04HONEY
265SUBSTITUTE
New York District Office (NYK-DO)
7/31/2012
36CCD04HONEY
265SUBSTITUTE
New York District Office (NYK-DO)
6/5/2012
21TGH03FIG, DRIED OR PASTE
249FILTHY
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Odem Gida Petrol Ve Orman Urunle's FDA import refusal history?

Odem Gida Petrol Ve Orman Urunle (FEI: 3008733114) has 8 FDA import refusal record(s) in our database, spanning from 6/5/2012 to 5/23/2013.

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. Odem Gida Petrol Ve Orman Urunle's FEI number is 3008733114.

What types of violations has Odem Gida Petrol Ve Orman Urunle received?

Odem Gida Petrol Ve Orman Urunle has been cited for 9 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 Odem Gida Petrol Ve Orman Urunle come from?

All FDA import refusal data for Odem Gida Petrol Ve Orman Urunle 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.