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Datax-Ohmedia Divison

⚠️ Moderate Risk

FEI: 3004090973 • Omhmeda • FINLAND

FEI

FEI Number

3004090973

📍

Location

Omhmeda

🇫🇮

Country

FINLAND
🏢

Address

Po Box 900, , Omhmeda, , Finland

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
8/22/2003
Latest Refusal
8/22/2003
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

3413×

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).

5083×

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
8/22/2003
80LHATIMER FOR DIAGNOSTIC USE
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/22/2003
80LHATIMER FOR DIAGNOSTIC USE
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
8/22/2003
80LHATIMER FOR DIAGNOSTIC USE
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Datax-Ohmedia Divison's FDA import refusal history?

Datax-Ohmedia Divison (FEI: 3004090973) has 3 FDA import refusal record(s) in our database, spanning from 8/22/2003 to 8/22/2003.

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. Datax-Ohmedia Divison's FEI number is 3004090973.

What types of violations has Datax-Ohmedia Divison received?

Datax-Ohmedia Divison 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 Datax-Ohmedia Divison come from?

All FDA import refusal data for Datax-Ohmedia Divison 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.