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Ustar Biotechnologies (Hangzhou) Ltd.

⚠️ Moderate Risk

FEI: 3021775806 • Hangzhou, Zhejiang • CHINA

FEI

FEI Number

3021775806

📍

Location

Hangzhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

Building 2 F/6, Binjiang, Hangzhou, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

46.4
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
8/20/2025
Latest Refusal
4/27/2022
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
Refusal Volume
17.7×30%
Recency
77.5×20%
Frequency
6.0×10%
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).

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).

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.

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
8/20/2025
75NAKSYSTEM, TEST, BIOTINIDASE
118NOT LISTED
3280FRNMFGREG
Division of Northeast Imports (DNEI)
4/27/2022
83QLWCOVID-19 TEST HOME COLLECTION KIT DEVICES
237NO PMA
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Ustar Biotechnologies (Hangzhou) Ltd.'s FDA import refusal history?

Ustar Biotechnologies (Hangzhou) Ltd. (FEI: 3021775806) has 2 FDA import refusal record(s) in our database, spanning from 4/27/2022 to 8/20/2025.

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. Ustar Biotechnologies (Hangzhou) Ltd.'s FEI number is 3021775806.

What types of violations has Ustar Biotechnologies (Hangzhou) Ltd. received?

Ustar Biotechnologies (Hangzhou) 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 Ustar Biotechnologies (Hangzhou) Ltd. come from?

All FDA import refusal data for Ustar Biotechnologies (Hangzhou) 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.