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Icare Finland Oy

⚠️ Moderate Risk

FEI: 3005324856 • Vantaa, Uusimaa • FINLAND

FEI

FEI Number

3005324856

📍

Location

Vantaa, Uusimaa

🇫🇮

Country

FINLAND
🏢

Address

Ayritie 22, , Vantaa, Uusimaa, Finland

Moderate Risk

FDA Import Risk Assessment

37.8
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
5/31/2024
Latest Refusal
2/2/2011
Earliest Refusal

Score Breakdown

Violation Severity
43.3×40%
Refusal Volume
22.3×30%
Recency
67.7×20%
Frequency
2.3×10%
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

3412×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
5/31/2024
86HKYTONOMETER, MANUAL
341REGISTERED
Division of Southeast Imports (DSEI)
3/25/2022
86HKXTONOMETER, AC-POWERED
341REGISTERED
Division of Southeast Imports (DSEI)
2/2/2011
86HKYTONOMETER, MANUAL
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Icare Finland Oy's FDA import refusal history?

Icare Finland Oy (FEI: 3005324856) has 3 FDA import refusal record(s) in our database, spanning from 2/2/2011 to 5/31/2024.

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. Icare Finland Oy's FEI number is 3005324856.

What types of violations has Icare Finland Oy received?

Icare Finland Oy 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 Icare Finland Oy come from?

All FDA import refusal data for Icare Finland Oy 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.