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RAPIGEN

⚠️ Moderate Risk

FEI: 3021637273 • Kyungki • SOUTH KOREA

FEI

FEI Number

3021637273

📍

Location

Kyungki

🇰🇷
🏢

Address

16648 Kwunsungu Sanupro155 Bungil 161, Suwon, , Kyungki, , South Korea

Moderate Risk

FDA Import Risk Assessment

34.2
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
3/12/2022
Latest Refusal
3/12/2022
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
9.3×20%
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

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
3/12/2022
83QLWCOVID-19 TEST HOME COLLECTION KIT DEVICES
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is RAPIGEN's FDA import refusal history?

RAPIGEN (FEI: 3021637273) has 1 FDA import refusal record(s) in our database, spanning from 3/12/2022 to 3/12/2022.

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. RAPIGEN's FEI number is 3021637273.

What types of violations has RAPIGEN received?

RAPIGEN has been cited for 1 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 RAPIGEN come from?

All FDA import refusal data for RAPIGEN 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.