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Wuhan UNScience Biotechnology Co Ltd

⚠️ Moderate Risk

FEI: 3016884874 • Wuhan, Hubei • CHINA

FEI

FEI Number

3016884874

📍

Location

Wuhan, Hubei

🇨🇳

Country

CHINA
🏢

Address

Building B18, 2nd Phase of Biomedical Park, #858 GaoXin Rd, Wuhan, Hubei, China

Moderate Risk

FDA Import Risk Assessment

43.4
LowModerateHighCritical

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

Statistics

7
Total Refusals
4
Unique Violations
2/5/2021
Latest Refusal
6/10/2020
Earliest Refusal

Score Breakdown

Violation Severity
66.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

5086×

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.

162×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

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).

32801×

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.

Refusal History

DateProductViolationsDivision
2/5/2021
83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
508NO 510(K)
Division of Southeast Imports (DSEI)
1/29/2021
83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
508NO 510(K)
Division of Southeast Imports (DSEI)
9/29/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
8/19/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
16DIRECTIONS
508NO 510(K)
Division of Southeast Imports (DSEI)
8/17/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
16DIRECTIONS
508NO 510(K)
Division of Southeast Imports (DSEI)
6/15/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
508NO 510(K)
Division of Southeast Imports (DSEI)
6/10/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Wuhan UNScience Biotechnology Co Ltd's FDA import refusal history?

Wuhan UNScience Biotechnology Co Ltd (FEI: 3016884874) has 7 FDA import refusal record(s) in our database, spanning from 6/10/2020 to 2/5/2021.

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. Wuhan UNScience Biotechnology Co Ltd's FEI number is 3016884874.

What types of violations has Wuhan UNScience Biotechnology Co Ltd received?

Wuhan UNScience Biotechnology 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 Wuhan UNScience Biotechnology Co Ltd come from?

All FDA import refusal data for Wuhan UNScience Biotechnology 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.