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SUER GIDA SANAYI VE DIS TICARETAS

⚠️ High Risk

FEI: 3016726914 • Germencik Aydin • TURKEY

FEI

FEI Number

3016726914

📍

Location

Germencik Aydin

🇹🇷

Country

TURKEY
🏢

Address

Ortaklar Organize Saniti Bolgesi 1.000 Cadde, , Germencik Aydin, , Turkey

High Risk

FDA Import Risk Assessment

59.9
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

2
Total Refusals
1
Unique Violations
3/27/2025
Latest Refusal
8/25/2022
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
17.7×30%
Recency
68.9×20%
Frequency
7.7×10%
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

2412×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
3/27/2025
21TFH03FIG, DRIED OR PASTE
241PESTICIDE
Division of Northern Border Imports (DNBI)
8/25/2022
21TFH03FIG, DRIED OR PASTE
241PESTICIDE
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is SUER GIDA SANAYI VE DIS TICARETAS's FDA import refusal history?

SUER GIDA SANAYI VE DIS TICARETAS (FEI: 3016726914) has 2 FDA import refusal record(s) in our database, spanning from 8/25/2022 to 3/27/2025.

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. SUER GIDA SANAYI VE DIS TICARETAS's FEI number is 3016726914.

What types of violations has SUER GIDA SANAYI VE DIS TICARETAS received?

SUER GIDA SANAYI VE DIS TICARETAS 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 SUER GIDA SANAYI VE DIS TICARETAS come from?

All FDA import refusal data for SUER GIDA SANAYI VE DIS TICARETAS 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.