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SHENZHEN SOGA TECHNOLOGY CO.,LTD

⚠️ Moderate Risk

FEI: 3030655344 • Shenzhen • CHINA

FEI

FEI Number

3030655344

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Building 188 Room 9010, North St, Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

43.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
5/6/2024
Latest Refusal
5/6/2024
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
22.3×30%
Recency
51.3×20%
Frequency
30.0×10%
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

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.

473×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

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.

Refusal History

DateProductViolationsDivision
5/6/2024
76EIBSYRINGE, IRRIGATING (DENTAL)
118NOT LISTED
3280FRNMFGREG
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)
5/6/2024
76ELCSCALER, ULTRASONIC
118NOT LISTED
3280FRNMFGREG
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)
5/6/2024
76NVKLASER, DENTAL, SOFT TISSUE
118NOT LISTED
3280FRNMFGREG
47NON STD
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

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

SHENZHEN SOGA TECHNOLOGY CO.,LTD (FEI: 3030655344) has 3 FDA import refusal record(s) in our database, spanning from 5/6/2024 to 5/6/2024.

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 SOGA TECHNOLOGY CO.,LTD's FEI number is 3030655344.

What types of violations has SHENZHEN SOGA TECHNOLOGY CO.,LTD received?

SHENZHEN SOGA 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 SHENZHEN SOGA TECHNOLOGY CO.,LTD come from?

All FDA import refusal data for SHENZHEN SOGA 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.