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Medical Supply Co.,Ltd

⚠️ Moderate Risk

FEI: 3004753864 • Seoul • SOUTH KOREA

FEI

FEI Number

3004753864

📍

Location

Seoul

🇰🇷
🏢

Address

3f Chilsung Bldg,155, Karak, , Seoul, , South Korea

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

5
Total Refusals
5
Unique Violations
9/11/2013
Latest Refusal
1/31/2005
Earliest Refusal

Score Breakdown

Violation Severity
52.7×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
5.8×10%
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

1185×

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).

5085×

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.

32804×

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.

37414×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

4764×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
9/11/2013
73DQAOXIMETER
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
476NO REGISTR
508NO 510(K)
Seattle District Office (SEA-DO)
9/11/2013
73DQAOXIMETER
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
476NO REGISTR
508NO 510(K)
Seattle District Office (SEA-DO)
9/11/2013
73DQAOXIMETER
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
476NO REGISTR
508NO 510(K)
Seattle District Office (SEA-DO)
9/11/2013
73DQAOXIMETER
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
476NO REGISTR
508NO 510(K)
Seattle District Office (SEA-DO)
1/31/2005
90IYNSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
118NOT LISTED
508NO 510(K)
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Medical Supply Co.,Ltd's FDA import refusal history?

Medical Supply Co.,Ltd (FEI: 3004753864) has 5 FDA import refusal record(s) in our database, spanning from 1/31/2005 to 9/11/2013.

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. Medical Supply Co.,Ltd's FEI number is 3004753864.

What types of violations has Medical Supply Co.,Ltd received?

Medical Supply Co.,Ltd has been cited for 5 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 Medical Supply Co.,Ltd come from?

All FDA import refusal data for Medical Supply Co.,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.