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Guangzhou Konmison Electronic Technology Co., Limited

⚠️ Moderate Risk

FEI: 3012935920 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3012935920

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Guangyi Business Center E-202, Baiyun Avenue North 86 Baiyun, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

42.7
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
8/27/2024
Latest Refusal
3/30/2015
Earliest Refusal

Score Breakdown

Violation Severity
57.5×40%
Refusal Volume
25.9×30%
Recency
57.7×20%
Frequency
4.3×10%
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

5084×

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.

1182×

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.

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
8/27/2024
89PHWCOLD PACK AND VIBRATING MASSAGER
508NO 510(K)
Division of Southeast Imports (DSEI)
4/9/2020
79ONFPOWERED LIGHT BASED NON-LASER SURGICAL INSTRUMENT WITH THERMAL EFFECT
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
7/25/2017
89PHWCOLD PACK AND VIBRATING MASSAGER
508NO 510(K)
Division of Northern Border Imports (DNBI)
3/30/2015
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
341REGISTERED
508NO 510(K)
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Guangzhou Konmison Electronic Technology Co., Limited's FDA import refusal history?

Guangzhou Konmison Electronic Technology Co., Limited (FEI: 3012935920) has 4 FDA import refusal record(s) in our database, spanning from 3/30/2015 to 8/27/2024.

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. Guangzhou Konmison Electronic Technology Co., Limited's FEI number is 3012935920.

What types of violations has Guangzhou Konmison Electronic Technology Co., Limited received?

Guangzhou Konmison Electronic Technology Co., Limited 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 Guangzhou Konmison Electronic Technology Co., Limited come from?

All FDA import refusal data for Guangzhou Konmison Electronic Technology Co., Limited 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.