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AURAD IFTIKHAR

⚠️ Moderate Risk

FEI: 3014587809 • Selden, NY • UNITED STATES

FEI

FEI Number

3014587809

📍

Location

Selden, NY

🇺🇸
🏢

Address

18 Laurelton Ave, , Selden, NY, United States

Moderate Risk

FDA Import Risk Assessment

41.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
8/23/2018
Latest Refusal
8/23/2018
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

2903×

DE IMP GMP

The article is subject to refusal of admission pursuant to section 801(a)(1) in that it appears that the methods used in, or the facilities or controls used for, the manufacture of the device do not conform to the applicable requirements of section 520(f).

Refusal History

DateProductViolationsDivision
8/23/2018
76EMNSCALER, PERIODONTIC
290DE IMP GMP
Division of Northern Border Imports (DNBI)
8/23/2018
79LRWSCISSORS, GENERAL USE, SURGICAL
290DE IMP GMP
Division of Northern Border Imports (DNBI)
8/23/2018
79HTEELEVATOR
290DE IMP GMP
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is AURAD IFTIKHAR's FDA import refusal history?

AURAD IFTIKHAR (FEI: 3014587809) has 3 FDA import refusal record(s) in our database, spanning from 8/23/2018 to 8/23/2018.

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. AURAD IFTIKHAR's FEI number is 3014587809.

What types of violations has AURAD IFTIKHAR received?

AURAD IFTIKHAR 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 AURAD IFTIKHAR come from?

All FDA import refusal data for AURAD IFTIKHAR 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.