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Bio Focus Co. Ltd.

⚠️ Moderate Risk

FEI: 3005841978 • Uiwang-si, Geonggi-do • SOUTH KOREA

FEI

FEI Number

3005841978

📍

Location

Uiwang-si, Geonggi-do

🇰🇷
🏢

Address

Deahyun Technoworld, Ojeon-dong, , Uiwang-si, Geonggi-do, South Korea

Moderate Risk

FDA Import Risk Assessment

30.1
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
4/23/2012
Latest Refusal
4/23/2012
Earliest Refusal

Score Breakdown

Violation Severity
51.1×40%
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

1183×

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).

3413×

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).

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.

2371×

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).

Refusal History

DateProductViolationsDivision
4/23/2012
83OAXPLASMODIUM SPP. DETECTION REAGENTS
118NOT LISTED
341REGISTERED
508NO 510(K)
Seattle District Office (SEA-DO)
4/23/2012
83GMQANTIGENS, NONTREPONEMAL, ALL
118NOT LISTED
341REGISTERED
508NO 510(K)
Seattle District Office (SEA-DO)
4/23/2012
82MZFTEST, HIV DETECTION
118NOT LISTED
237NO PMA
341REGISTERED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Bio Focus Co. Ltd.'s FDA import refusal history?

Bio Focus Co. Ltd. (FEI: 3005841978) has 3 FDA import refusal record(s) in our database, spanning from 4/23/2012 to 4/23/2012.

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. Bio Focus Co. Ltd.'s FEI number is 3005841978.

What types of violations has Bio Focus Co. Ltd. received?

Bio Focus Co. 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 Bio Focus Co. Ltd. come from?

All FDA import refusal data for Bio Focus 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.