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SUNWOO I&T

⚠️ Moderate Risk

FEI: 3009491199 • Seoul, Seoul • SOUTH KOREA

FEI

FEI Number

3009491199

📍

Location

Seoul, Seoul

🇰🇷
🏢

Address

1f, 371-22 Kongkoo B/D, Shinsoo-Dong, Mapo-Gu, Seoul, Seoul, South Korea

Moderate Risk

FDA Import Risk Assessment

35.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
3
Unique Violations
4/23/2014
Latest Refusal
5/15/2013
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(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).

5081×

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
4/23/2014
79GDFGUIDE, NEEDLE, SURGICAL
237NO PMA
508NO 510(K)
Seattle District Office (SEA-DO)
2/21/2014
79GFEBRUSH, DERMABRASION
237NO PMA
Cincinnati District Office (CIN-DO)
5/15/2013
79GFEBRUSH, DERMABRASION
341REGISTERED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is SUNWOO I&T's FDA import refusal history?

SUNWOO I&T (FEI: 3009491199) has 3 FDA import refusal record(s) in our database, spanning from 5/15/2013 to 4/23/2014.

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. SUNWOO I&T's FEI number is 3009491199.

What types of violations has SUNWOO I&T received?

SUNWOO I&T 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 SUNWOO I&T come from?

All FDA import refusal data for SUNWOO I&T 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.