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GORGEOUS BEAUTY EQUIPMENT MANUFACTU

⚠️ Moderate Risk

FEI: 3018472490 • Xian • CHINA

FEI

FEI Number

3018472490

📍

Location

Xian

🇨🇳

Country

CHINA
🏢

Address

1219 Block B, Huadi Jin, Welyang District, Xian, , China

Moderate Risk

FDA Import Risk Assessment

25.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
5/14/2021
Latest Refusal
5/14/2021
Earliest Refusal

Score Breakdown

Violation Severity
52.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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).

2781×

NO TAG

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 to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).

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.

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

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
5/14/2021
77EWGLASER, ENT MICROSURGICAL CARBON-DIOXIDE
118NOT LISTED
278NO TAG
3280FRNMFGREG
476NO REGISTR
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is GORGEOUS BEAUTY EQUIPMENT MANUFACTU's FDA import refusal history?

GORGEOUS BEAUTY EQUIPMENT MANUFACTU (FEI: 3018472490) has 1 FDA import refusal record(s) in our database, spanning from 5/14/2021 to 5/14/2021.

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. GORGEOUS BEAUTY EQUIPMENT MANUFACTU's FEI number is 3018472490.

What types of violations has GORGEOUS BEAUTY EQUIPMENT MANUFACTU received?

GORGEOUS BEAUTY EQUIPMENT MANUFACTU 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 GORGEOUS BEAUTY EQUIPMENT MANUFACTU come from?

All FDA import refusal data for GORGEOUS BEAUTY EQUIPMENT MANUFACTU 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.