ImportRefusal LogoImportRefusal

CANKATAN GIDA SANAYI VE TICARETLIM

⚠️ Moderate Risk

FEI: 3023954122 • Isletim Kayat • TURKEY

FEI

FEI Number

3023954122

📍

Location

Isletim Kayat

🇹🇷

Country

TURKEY
🏢

Address

72/2/A Buyukkayacik Osb, , Isletim Kayat, , Turkey

Moderate Risk

FDA Import Risk Assessment

44.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
10/28/2022
Latest Refusal
10/28/2022
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
11.2×30%
Recency
21.9×20%
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

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
10/28/2022
54YYY10ROYAL JELLY (VIT/MIN/PROTEIN/UNCONVENTIONAL DIETARY SPEC FOR HUMAN/ANIMAL, N.E.C.)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is CANKATAN GIDA SANAYI VE TICARETLIM's FDA import refusal history?

CANKATAN GIDA SANAYI VE TICARETLIM (FEI: 3023954122) has 1 FDA import refusal record(s) in our database, spanning from 10/28/2022 to 10/28/2022.

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. CANKATAN GIDA SANAYI VE TICARETLIM's FEI number is 3023954122.

What types of violations has CANKATAN GIDA SANAYI VE TICARETLIM received?

CANKATAN GIDA SANAYI VE TICARETLIM 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 CANKATAN GIDA SANAYI VE TICARETLIM come from?

All FDA import refusal data for CANKATAN GIDA SANAYI VE TICARETLIM 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.