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SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI

⚠️ Moderate Risk

FEI: 3004665382 • BURSA, TR-16 • TURKEY

FEI

FEI Number

3004665382

📍

Location

BURSA, TR-16

🇹🇷

Country

TURKEY
🏢

Address

DEGIRMENLI KIZIK MAH CAKMAK SOK NO 3, YILDIRIM, BURSA, TR-16, Turkey

Moderate Risk

FDA Import Risk Assessment

28.8
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
3/20/2012
Latest Refusal
5/4/2011
Earliest Refusal

Score Breakdown

Violation Severity
47.8×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

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.

4732×

LABELING

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

832×

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.

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)).

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.

Refusal History

DateProductViolationsDivision
3/20/2012
23BCT04CHESTNUT, SHELLED
473LABELING
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
3/20/2012
23BCT04CHESTNUT, SHELLED
473LABELING
482NUTRIT LBL
83NO PROCESS
New York District Office (NYK-DO)
5/4/2011
23BGT04CHESTNUT, SHELLED
324NO ENGLISH
328USUAL NAME
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI's FDA import refusal history?

SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI (FEI: 3004665382) has 3 FDA import refusal record(s) in our database, spanning from 5/4/2011 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. SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI's FEI number is 3004665382.

What types of violations has SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI received?

SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI has been cited for 5 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 SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI come from?

All FDA import refusal data for SELAHATTIN DAGLI GIDA SEKERLEME SAN VE TIC LTD STI 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.