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Artec Systems Group

⚠️ Moderate Risk

FEI: 3003249533 • Port Washington, NY • UNITED STATES

FEI

FEI Number

3003249533

📍

Location

Port Washington, NY

🇺🇸
🏢

Address

99 Seaview Blvd, , Port Washington, NY, United States

Moderate Risk

FDA Import Risk Assessment

33.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
9/15/2004
Latest Refusal
9/15/2004
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

112×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

4732×

LABELING

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

Refusal History

DateProductViolationsDivision
9/15/2004
53FD06HAIR LIGHTENERS, WITH COLOR (HAIR COLORING PREPARATIONS)
11UNSAFE COL
473LABELING
New York District Office (NYK-DO)
9/15/2004
53FD06HAIR LIGHTENERS, WITH COLOR (HAIR COLORING PREPARATIONS)
11UNSAFE COL
473LABELING
New York District Office (NYK-DO)

Frequently Asked Questions

What is Artec Systems Group's FDA import refusal history?

Artec Systems Group (FEI: 3003249533) has 2 FDA import refusal record(s) in our database, spanning from 9/15/2004 to 9/15/2004.

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. Artec Systems Group's FEI number is 3003249533.

What types of violations has Artec Systems Group received?

Artec Systems Group has been cited for 2 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 Artec Systems Group come from?

All FDA import refusal data for Artec Systems Group 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.