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Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1

⚠️ Moderate Risk

FEI: 3015290259 • Akhisar, Manisa • TURKEY

FEI

FEI Number

3015290259

📍

Location

Akhisar, Manisa

🇹🇷

Country

TURKEY
🏢

Address

Akhisar Organized Industrial 3rd St. No 8 Kayalioglu Neighborhood, , Akhisar, Manisa, Turkey

Moderate Risk

FDA Import Risk Assessment

31.4
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
10/29/2024
Latest Refusal
10/29/2024
Earliest Refusal

Score Breakdown

Violation Severity
36.7×40%
Refusal Volume
11.2×30%
Recency
62.0×20%
Frequency
10.0×10%
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

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.

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.

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
10/29/2024
33MGT01GEL CUPS, FRUIT FLAVORED
218LIST INGRE
320LACKS FIRM
482NUTRIT LBL
Division of Southwest Imports (DSWI)

Frequently Asked Questions

What is Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1's FDA import refusal history?

Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 (FEI: 3015290259) has 1 FDA import refusal record(s) in our database, spanning from 10/29/2024 to 10/29/2024.

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. Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1's FEI number is 3015290259.

What types of violations has Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 received?

Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 has been cited for 3 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 Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 come from?

All FDA import refusal data for Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 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.