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SAI GROUP PROJE YONETIMI SANAYI

⚠️ Moderate Risk

FEI: 3020727044 • Buyukcekmece • TURKEY

FEI

FEI Number

3020727044

📍

Location

Buyukcekmece

🇹🇷

Country

TURKEY
🏢

Address

Pinartepe Mah, Turgut Ozal 1 Cad Ticaret Limited Sirketi, Buyukcekmece, , Turkey

Moderate Risk

FDA Import Risk Assessment

33.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
8/9/2023
Latest Refusal
8/9/2023
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
22.3×30%
Recency
36.4×20%
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

4733×

LABELING

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

Refusal History

DateProductViolationsDivision
8/9/2023
03JGT02CHOCOLATE FILLED/ICED COOKIES,BISCUITS AND WAFERS
473LABELING
Division of Southeast Imports (DSEI)
8/9/2023
03JGT02CHOCOLATE FILLED/ICED COOKIES,BISCUITS AND WAFERS
473LABELING
Division of Southeast Imports (DSEI)
8/9/2023
03JGT02CHOCOLATE FILLED/ICED COOKIES,BISCUITS AND WAFERS
473LABELING
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SAI GROUP PROJE YONETIMI SANAYI's FDA import refusal history?

SAI GROUP PROJE YONETIMI SANAYI (FEI: 3020727044) has 3 FDA import refusal record(s) in our database, spanning from 8/9/2023 to 8/9/2023.

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. SAI GROUP PROJE YONETIMI SANAYI's FEI number is 3020727044.

What types of violations has SAI GROUP PROJE YONETIMI SANAYI received?

SAI GROUP PROJE YONETIMI SANAYI has been cited for 1 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 SAI GROUP PROJE YONETIMI SANAYI come from?

All FDA import refusal data for SAI GROUP PROJE YONETIMI SANAYI 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.