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MRG PAKETLEME GIDA AMBALAJ URETIM SAN.LTD.STI

⚠️ Moderate Risk

FEI: 3016255781 • Ankara, Ankara • TURKEY

FEI

FEI Number

3016255781

📍

Location

Ankara, Ankara

🇹🇷

Country

TURKEY
🏢

Address

Anadolu Organized Industrial Zone 13 St.No.11 Malikoy Sincan, , Ankara, Ankara, Turkey

Moderate Risk

FDA Import Risk Assessment

41.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
12/22/2021
Latest Refusal
12/22/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
4.9×20%
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

1811×

UNDER PRC

The article appears to have inadequate processing in having been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
12/22/2021
24FCE20CUCUMBERS (FRUIT USED AS VEGETABLE)
181UNDER PRC
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MRG PAKETLEME GIDA AMBALAJ URETIM SAN.LTD.STI's FDA import refusal history?

MRG PAKETLEME GIDA AMBALAJ URETIM SAN.LTD.STI (FEI: 3016255781) has 1 FDA import refusal record(s) in our database, spanning from 12/22/2021 to 12/22/2021.

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. MRG PAKETLEME GIDA AMBALAJ URETIM SAN.LTD.STI's FEI number is 3016255781.

What types of violations has MRG PAKETLEME GIDA AMBALAJ URETIM SAN.LTD.STI received?

MRG PAKETLEME GIDA AMBALAJ URETIM SAN.LTD.STI 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 MRG PAKETLEME GIDA AMBALAJ URETIM SAN.LTD.STI come from?

All FDA import refusal data for MRG PAKETLEME GIDA AMBALAJ URETIM SAN.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.