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XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY CO.,LTD.

⚠️ Moderate Risk

FEI: 3012365608 • Xiamen, Fujian • CHINA

FEI

FEI Number

3012365608

📍

Location

Xiamen, Fujian

🇨🇳

Country

CHINA
🏢

Address

F 2-5, Simingyuan No.118, Xiamen, Fujian, China

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

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

Statistics

5
Total Refusals
4
Unique Violations
2/22/2024
Latest Refusal
11/16/2022
Earliest Refusal

Score Breakdown

Violation Severity
52.2×40%
Refusal Volume
28.8×30%
Recency
47.8×20%
Frequency
39.4×10%
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

5083×

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).

32802×

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).

Refusal History

DateProductViolationsDivision
2/22/2024
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
508NO 510(K)
Division of Northeast Imports (DNEI)
9/8/2023
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
508NO 510(K)
Division of West Coast Imports (DWCI)
8/22/2023
85MGIASPIRATOR, ULTRASONIC
118NOT LISTED
Division of West Coast Imports (DWCI)
8/18/2023
79BTAPUMP, PORTABLE, ASPIRATION (MANUAL OR POWERED)
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
11/16/2022
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY CO.,LTD.'s FDA import refusal history?

XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY CO.,LTD. (FEI: 3012365608) has 5 FDA import refusal record(s) in our database, spanning from 11/16/2022 to 2/22/2024.

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. XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY CO.,LTD.'s FEI number is 3012365608.

What types of violations has XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY CO.,LTD. received?

XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY CO.,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 XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY CO.,LTD. come from?

All FDA import refusal data for XIAMEN HIGH TOP ELECTRONIC TECHNOLOGY 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.