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GUANGDONG SEYOUSE TECHNOLOGICAL

⚠️ Moderate Risk

FEI: 3016715145 • Dongguan • CHINA

FEI

FEI Number

3016715145

📍

Location

Dongguan

🇨🇳

Country

CHINA
🏢

Address

Bldg 3, No 8 Chiling Ind, Dongguan, , China

Moderate Risk

FDA Import Risk Assessment

41.3
LowModerateHighCritical

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

Statistics

7
Total Refusals
3
Unique Violations
12/2/2020
Latest Refusal
12/1/2020
Earliest Refusal

Score Breakdown

Violation Severity
60.8×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

5087×

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.

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.

Refusal History

DateProductViolationsDivision
12/2/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/1/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/1/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/1/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/1/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/1/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)
12/1/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is GUANGDONG SEYOUSE TECHNOLOGICAL's FDA import refusal history?

GUANGDONG SEYOUSE TECHNOLOGICAL (FEI: 3016715145) has 7 FDA import refusal record(s) in our database, spanning from 12/1/2020 to 12/2/2020.

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. GUANGDONG SEYOUSE TECHNOLOGICAL's FEI number is 3016715145.

What types of violations has GUANGDONG SEYOUSE TECHNOLOGICAL received?

GUANGDONG SEYOUSE TECHNOLOGICAL has been cited for 3 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 GUANGDONG SEYOUSE TECHNOLOGICAL come from?

All FDA import refusal data for GUANGDONG SEYOUSE TECHNOLOGICAL 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.