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Perfetti van Melle Gida Sinayi Ve Ticaret A.S.

⚠️ Moderate Risk

FEI: 3003714245 • Esenyurt, Istanbul • TURKEY

FEI

FEI Number

3003714245

📍

Location

Esenyurt, Istanbul

🇹🇷

Country

TURKEY
🏢

Address

Osmangazi Mahallesi, Gazi Caddesi No 15, Esenyurt, Istanbul, Turkey

Moderate Risk

FDA Import Risk Assessment

36.8
LowModerateHighCritical

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

Statistics

14
Total Refusals
6
Unique Violations
11/18/2016
Latest Refusal
6/26/2009
Earliest Refusal

Score Breakdown

Violation Severity
54.7×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
18.9×10%
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

2188×

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.

115×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2741×

COLOR LBLG

The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.

3241×

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)).

33201×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

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.

Refusal History

DateProductViolationsDivision
11/18/2016
33LGT11MINT CANDY, SOFT, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
274COLOR LBLG
3320TRANSFAT
Division of Southeast Imports (DSEI)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/13/2016
33UGT02CHEWING GUM (WITHOUT CHOCOLATE)
218LIST INGRE
New York District Office (NYK-DO)
1/25/2012
33JGT07JELLIED CANDY, SOFT (JELLY BEANS, GUM DROPS, ETC.), WITH FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Florida District Office (FLA-DO)
12/13/2011
33UFT01BUBBLE GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
New Orleans District Office (NOL-DO)
12/13/2011
33UFT01BUBBLE GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
New Orleans District Office (NOL-DO)
10/23/2009
33UYY02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
324NO ENGLISH
Division of Southeast Imports (DSEI)
6/26/2009
33UAY02CHEWING GUM (WITHOUT CHOCOLATE)
11UNSAFE COL
482NUTRIT LBL
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Perfetti van Melle Gida Sinayi Ve Ticaret A.S.'s FDA import refusal history?

Perfetti van Melle Gida Sinayi Ve Ticaret A.S. (FEI: 3003714245) has 14 FDA import refusal record(s) in our database, spanning from 6/26/2009 to 11/18/2016.

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. Perfetti van Melle Gida Sinayi Ve Ticaret A.S.'s FEI number is 3003714245.

What types of violations has Perfetti van Melle Gida Sinayi Ve Ticaret A.S. received?

Perfetti van Melle Gida Sinayi Ve Ticaret A.S. 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 Perfetti van Melle Gida Sinayi Ve Ticaret A.S. come from?

All FDA import refusal data for Perfetti van Melle Gida Sinayi Ve Ticaret 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.