Peyman Kuruyemis Gida San. ve Tic. A. S.
⚠️ Moderate Risk
FEI: 3008673651 • Odunpazari, Eskisehir • TURKEY
FEI Number
3008673651
Location
Odunpazari, Eskisehir
Country
TURKEYAddress
Organize Sanayi Bolgesi 9. Cad. No. 16, , Odunpazari, Eskisehir, Turkey
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
INCONSPICU
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)).
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.
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
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)).
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
PB-FOOD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance, lead, which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/29/2022 | 20BHT10RAISINS, DRIED OR PASTE | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 8/7/2017 | 21HGH01APRICOT, DRIED OR PASTE | Division of Southwest Imports (DSWI) | |
| 8/7/2017 | 21TGH03FIG, DRIED OR PASTE | Division of Southwest Imports (DSWI) | |
| 8/7/2017 | 23RGT04SUNFLOWER SEED (EDIBLE SEED PASTE) | Division of Southwest Imports (DSWI) | |
| 8/7/2017 | 23RGT04SUNFLOWER SEED (EDIBLE SEED PASTE) | Division of Southwest Imports (DSWI) | |
| 6/12/2014 | 20BGH10RAISINS, DRIED OR PASTE | 3400PB-FOOD | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Peyman Kuruyemis Gida San. ve Tic. A. S.'s FDA import refusal history?
Peyman Kuruyemis Gida San. ve Tic. A. S. (FEI: 3008673651) has 6 FDA import refusal record(s) in our database, spanning from 6/12/2014 to 3/29/2022.
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. Peyman Kuruyemis Gida San. ve Tic. A. S.'s FEI number is 3008673651.
What types of violations has Peyman Kuruyemis Gida San. ve Tic. A. S. received?
Peyman Kuruyemis Gida San. ve Tic. A. S. has been cited for 8 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 Peyman Kuruyemis Gida San. ve Tic. A. S. come from?
All FDA import refusal data for Peyman Kuruyemis Gida 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.