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HANGZHOU BUS LOGISTICS TECHNOLOG

⚠️ Moderate Risk

FEI: 3013008884 • Hangzhou • CHINA

FEI

FEI Number

3013008884

📍

Location

Hangzhou

🇨🇳

Country

CHINA
🏢

Address

Buld 1 F 1, NO 109 Hongx, Hangzhou, , China

Moderate Risk

FDA Import Risk Assessment

32.4
LowModerateHighCritical

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

Statistics

5
Total Refusals
5
Unique Violations
3/8/2019
Latest Refusal
8/3/2017
Earliest Refusal

Score Breakdown

Violation Severity
51.5×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
31.4×10%
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

1185×

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).

32804×

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.

2352×

NOT IMPACT

The article appears to not have impact-resistant lenses in accordance with 21 CFR 801.410.

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
3/8/2019
79OVNSUTURE KIT
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
5/8/2018
73BZDVENTILATOR, NON-CONTINUOUS (RESPIRATOR)
118NOT LISTED
Division of Southeast Imports (DSEI)
9/15/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
9/11/2017
86HOISPECTACLE, MAGNIFYING
118NOT LISTED
235NOT IMPACT
3280FRNMFGREG
Division of Northern Border Imports (DNBI)
8/3/2017
86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE)
118NOT LISTED
3280FRNMFGREG
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is HANGZHOU BUS LOGISTICS TECHNOLOG's FDA import refusal history?

HANGZHOU BUS LOGISTICS TECHNOLOG (FEI: 3013008884) has 5 FDA import refusal record(s) in our database, spanning from 8/3/2017 to 3/8/2019.

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. HANGZHOU BUS LOGISTICS TECHNOLOG's FEI number is 3013008884.

What types of violations has HANGZHOU BUS LOGISTICS TECHNOLOG received?

HANGZHOU BUS LOGISTICS TECHNOLOG has been cited for 5 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 HANGZHOU BUS LOGISTICS TECHNOLOG come from?

All FDA import refusal data for HANGZHOU BUS LOGISTICS TECHNOLOG 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.