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WEIGAO MEDICAL INTERNATIONAL CO LTD

⚠️ Moderate Risk

FEI: 3014162214 • Weihai • CHINA

FEI

FEI Number

3014162214

📍

Location

Weihai

🇨🇳

Country

CHINA
🏢

Address

No 1 Weigao Road, High-Tech Industrial Development Zone, Weihai, , China

Moderate Risk

FDA Import Risk Assessment

42.4
LowModerateHighCritical

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

Statistics

5
Total Refusals
5
Unique Violations
10/18/2024
Latest Refusal
9/12/2018
Earliest Refusal

Score Breakdown

Violation Severity
51.8×40%
Refusal Volume
28.8×30%
Recency
60.9×20%
Frequency
8.2×10%
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

1183×

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).

32803×

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.

3412×

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).

4792×

DV QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.

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
10/18/2024
74DQOCATHETER, INTRAVASCULAR, DIAGNOSTIC
479DV QUALITY
Division of Northeast Imports (DNEI)
10/18/2024
74DQOCATHETER, INTRAVASCULAR, DIAGNOSTIC
479DV QUALITY
Division of Northeast Imports (DNEI)
7/2/2019
80MEGSYRINGE, ANTISTICK
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
9/12/2018
79GEACANNULA, SURGICAL, GENERAL & PLASTIC SURGERY
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
9/12/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is WEIGAO MEDICAL INTERNATIONAL CO LTD's FDA import refusal history?

WEIGAO MEDICAL INTERNATIONAL CO LTD (FEI: 3014162214) has 5 FDA import refusal record(s) in our database, spanning from 9/12/2018 to 10/18/2024.

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. WEIGAO MEDICAL INTERNATIONAL CO LTD's FEI number is 3014162214.

What types of violations has WEIGAO MEDICAL INTERNATIONAL CO LTD received?

WEIGAO MEDICAL INTERNATIONAL CO LTD 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 WEIGAO MEDICAL INTERNATIONAL CO LTD come from?

All FDA import refusal data for WEIGAO MEDICAL INTERNATIONAL 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.