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GUANGZHOU OFAN BEAUTY EQUIPMENTCO LTD

⚠️ Moderate Risk

FEI: 3021842553 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3021842553

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Sci-Info Park, No. 8 Helong Road, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

31.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
7
Unique Violations
4/19/2022
Latest Refusal
4/19/2022
Earliest Refusal

Score Breakdown

Violation Severity
55.7×40%
Refusal Volume
11.2×30%
Recency
25.4×20%
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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

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.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

4841×

DV NAME

The article appears to be a device and its labeling fails to bear the proprietary or established name.

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
4/19/2022
79PBXMASSAGER, VACUUM, RADIO FREQUENCY INDUCED HEAT
118NOT LISTED
16DIRECTIONS
237NO PMA
3280FRNMFGREG
333LACKS FIRM
484DV NAME
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is GUANGZHOU OFAN BEAUTY EQUIPMENTCO LTD's FDA import refusal history?

GUANGZHOU OFAN BEAUTY EQUIPMENTCO LTD (FEI: 3021842553) has 1 FDA import refusal record(s) in our database, spanning from 4/19/2022 to 4/19/2022.

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 OFAN BEAUTY EQUIPMENTCO LTD's FEI number is 3021842553.

What types of violations has GUANGZHOU OFAN BEAUTY EQUIPMENTCO LTD received?

GUANGZHOU OFAN BEAUTY EQUIPMENTCO LTD has been cited for 7 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 OFAN BEAUTY EQUIPMENTCO LTD come from?

All FDA import refusal data for GUANGZHOU OFAN BEAUTY EQUIPMENTCO 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.