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REALTIME TECHNOLOGIES LTD

⚠️ Moderate Risk

FEI: 3013205791 • Dublin • IRELAND

FEI

FEI Number

3013205791

📍

Location

Dublin

🇮🇪

Country

IRELAND
🏢

Address

Realtime Building, Colonhaugh Business Pk, Dublin, , Ireland

Moderate Risk

FDA Import Risk Assessment

30.7
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
3/18/2020
Latest Refusal
9/30/2019
Earliest Refusal

Score Breakdown

Violation Severity
58.6×40%
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

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32802×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

5082×

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.

30811×

INVDEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a device for investigational use for which no exemption has been granted as prescribed by Section 520(g)

Refusal History

DateProductViolationsDivision
3/18/2020
84GZODEVICE, GALVANIC SKIN RESPONSE MEASUREMENT
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/30/2019
74DPSELECTROCARDIOGRAPH
118NOT LISTED
3081INVDEVICE
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is REALTIME TECHNOLOGIES LTD's FDA import refusal history?

REALTIME TECHNOLOGIES LTD (FEI: 3013205791) has 2 FDA import refusal record(s) in our database, spanning from 9/30/2019 to 3/18/2020.

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. REALTIME TECHNOLOGIES LTD's FEI number is 3013205791.

What types of violations has REALTIME TECHNOLOGIES LTD received?

REALTIME TECHNOLOGIES LTD has been cited for 4 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 REALTIME TECHNOLOGIES LTD come from?

All FDA import refusal data for REALTIME TECHNOLOGIES LTD 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.