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Lbs

⚠️ Moderate Risk

FEI: 3003443766 • Istanbul • TURKEY

FEI

FEI Number

3003443766

📍

Location

Istanbul

🇹🇷

Country

TURKEY
🏢

Address

Gida Sanayi Ve Dis Tic A.S., , Ikitelli, Istanbul, , Turkey

Moderate Risk

FDA Import Risk Assessment

30.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
6
Unique Violations
8/16/2002
Latest Refusal
8/16/2002
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
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

833×

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.

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.

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.

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.

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
8/16/2002
24KCT02OKRA, WITH SAUCE
320LACKS FIRM
321LACKS N/C
328USUAL NAME
473LABELING
482NUTRIT LBL
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/16/2002
37BEE99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/16/2002
37BEE99MULTIPLE FOOD SPECIALITIES, SIDE DISHES AND DESSERTS, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Lbs's FDA import refusal history?

Lbs (FEI: 3003443766) has 3 FDA import refusal record(s) in our database, spanning from 8/16/2002 to 8/16/2002.

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. Lbs's FEI number is 3003443766.

What types of violations has Lbs received?

Lbs 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 Lbs come from?

All FDA import refusal data for Lbs 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.