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HANGZHOU LEEKAI TECHNOLOGY CENTE

⚠️ Moderate Risk

FEI: 3030579330 • Hangzhou, Zhejiang • CHINA

FEI

FEI Number

3030579330

📍

Location

Hangzhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

88 Jiang Ling Road, , Hangzhou, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

38.6
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
5/15/2024
Latest Refusal
5/15/2024
Earliest Refusal

Score Breakdown

Violation Severity
52.5×40%
Refusal Volume
11.2×30%
Recency
66.4×20%
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

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.

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).

Refusal History

DateProductViolationsDivision
5/15/2024
74DQPKIT, BALLOON REPAIR, CATHETER
118NOT LISTED
237NO PMA
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HANGZHOU LEEKAI TECHNOLOGY CENTE's FDA import refusal history?

HANGZHOU LEEKAI TECHNOLOGY CENTE (FEI: 3030579330) has 1 FDA import refusal record(s) in our database, spanning from 5/15/2024 to 5/15/2024.

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 LEEKAI TECHNOLOGY CENTE's FEI number is 3030579330.

What types of violations has HANGZHOU LEEKAI TECHNOLOGY CENTE received?

HANGZHOU LEEKAI TECHNOLOGY CENTE 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 HANGZHOU LEEKAI TECHNOLOGY CENTE come from?

All FDA import refusal data for HANGZHOU LEEKAI TECHNOLOGY CENTE 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.