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SHENZHEN TECHNOLOGY CO LTD

⚠️ Moderate Risk

FEI: 3012678899 • Shenzhen, Guangdong • CHINA

FEI

FEI Number

3012678899

📍

Location

Shenzhen, Guangdong

🇨🇳

Country

CHINA
🏢

Address

No. 2 Yongteng Road, Shixin Community Shiyan Town, Bao an District, , Shenzhen, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

35.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
7/18/2024
Latest Refusal
7/18/2024
Earliest Refusal

Score Breakdown

Violation Severity
42.0×40%
Refusal Volume
11.2×30%
Recency
70.0×20%
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).

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).

39051×

3905

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
7/18/2024
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is SHENZHEN TECHNOLOGY CO LTD's FDA import refusal history?

SHENZHEN TECHNOLOGY CO LTD (FEI: 3012678899) has 1 FDA import refusal record(s) in our database, spanning from 7/18/2024 to 7/18/2024.

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. SHENZHEN TECHNOLOGY CO LTD's FEI number is 3012678899.

What types of violations has SHENZHEN TECHNOLOGY CO LTD received?

SHENZHEN TECHNOLOGY 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 SHENZHEN TECHNOLOGY CO LTD come from?

All FDA import refusal data for SHENZHEN 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.