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Ezmedicom

✅ Low Risk

FEI: 3007536361 • Seocho Gu • SOUTH KOREA

FEI

FEI Number

3007536361

📍

Location

Seocho Gu

🇰🇷
🏢

Address

1536 26 Seocho 3 Dong, , Seocho Gu, , South Korea

Low Risk

FDA Import Risk Assessment

19.0
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
3
Unique Violations
6/2/2009
Latest Refusal
6/2/2009
Earliest Refusal

Score Breakdown

Violation Severity
36.7×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1181×

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).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

3411×

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).

Refusal History

DateProductViolationsDivision
6/2/2009
78FONBAG, DRAINAGE, WITH ADHESIVE, OSTOMY
118NOT LISTED
3260NO ENGLISH
341REGISTERED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Ezmedicom's FDA import refusal history?

Ezmedicom (FEI: 3007536361) has 1 FDA import refusal record(s) in our database, spanning from 6/2/2009 to 6/2/2009.

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. Ezmedicom's FEI number is 3007536361.

What types of violations has Ezmedicom received?

Ezmedicom 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 Ezmedicom come from?

All FDA import refusal data for Ezmedicom 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.