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Guangzhou Jianglong Beauty Equipment Co Ltd

⚠️ Moderate Risk

FEI: 3010429459 • Baiyun District, Guangzhou • CHINA

FEI

FEI Number

3010429459

📍

Location

Baiyun District, Guangzhou

🇨🇳

Country

CHINA
🏢

Address

Floor 4 Building 7 Xiamao Industrial Zon, Jichang Road, Baiyun District, Guangzhou, China

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
11/5/2013
Latest Refusal
11/5/2013
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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).

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.

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.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
11/5/2013
79ONFPOWERED LIGHT BASED NON-LASER SURGICAL INSTRUMENT WITH THERMAL EFFECT
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
84RX DEVICE
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Guangzhou Jianglong Beauty Equipment Co Ltd's FDA import refusal history?

Guangzhou Jianglong Beauty Equipment Co Ltd (FEI: 3010429459) has 1 FDA import refusal record(s) in our database, spanning from 11/5/2013 to 11/5/2013.

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. Guangzhou Jianglong Beauty Equipment Co Ltd's FEI number is 3010429459.

What types of violations has Guangzhou Jianglong Beauty Equipment Co Ltd received?

Guangzhou Jianglong Beauty Equipment 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 Guangzhou Jianglong Beauty Equipment Co Ltd come from?

All FDA import refusal data for Guangzhou Jianglong Beauty Equipment 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.