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Siemens Healthineers Ltd.

⚠️ Moderate Risk

FEI: 3005150580 • Seongnam, Gyeonggi • SOUTH KOREA

FEI

FEI Number

3005150580

📍

Location

Seongnam, Gyeonggi

🇰🇷
🏢

Address

Jungwon, 2 Nd-3rd Floor, 143, Sunhwan-Ro, Seongnam, Gyeonggi, South Korea

Moderate Risk

FDA Import Risk Assessment

45.1
LowModerateHighCritical

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

Statistics

7
Total Refusals
3
Unique Violations
8/21/2024
Latest Refusal
5/16/2016
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
33.5×30%
Recency
57.9×20%
Frequency
8.5×10%
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

1186×

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).

32806×

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.

5086×

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
8/21/2024
74OBJCATHETER, ULTRASOUND, INTRAVASCULAR
3280FRNMFGREG
Division of Southeast Imports (DSEI)
4/8/2019
74OBJCATHETER, ULTRASOUND, INTRAVASCULAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
4/8/2019
74OBJCATHETER, ULTRASOUND, INTRAVASCULAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
4/8/2019
74OBJCATHETER, ULTRASOUND, INTRAVASCULAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
4/8/2019
74OBJCATHETER, ULTRASOUND, INTRAVASCULAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
4/8/2019
74OBJCATHETER, ULTRASOUND, INTRAVASCULAR
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
5/16/2016
90ITXTRANSDUCER, ULTRASONIC, DIAGNOSTIC
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Siemens Healthineers Ltd.'s FDA import refusal history?

Siemens Healthineers Ltd. (FEI: 3005150580) has 7 FDA import refusal record(s) in our database, spanning from 5/16/2016 to 8/21/2024.

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. Siemens Healthineers Ltd.'s FEI number is 3005150580.

What types of violations has Siemens Healthineers Ltd. received?

Siemens Healthineers Ltd. has been cited for 3 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 Siemens Healthineers Ltd. come from?

All FDA import refusal data for Siemens Healthineers 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.