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Kallum Beauty Care Products Co Ltd

⚠️ Moderate Risk

FEI: 3009829353 • Yanzhoush, Yandong • CHINA

FEI

FEI Number

3009829353

📍

Location

Yanzhoush, Yandong

🇨🇳

Country

CHINA
🏢

Address

215 Zhongshandadaoxi, , Yanzhoush, Yandong, China

Moderate Risk

FDA Import Risk Assessment

38.7
LowModerateHighCritical

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

Statistics

9
Total Refusals
3
Unique Violations
12/31/2012
Latest Refusal
12/31/2012
Earliest Refusal

Score Breakdown

Violation Severity
46.5×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

1189×

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).

3419×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

5085×

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
12/31/2012
84NYXSTIMULATOR, ELECTRICAL, TRANSCUTANEOUS, WITH LIMTED OUTPUT, FOR AESTHETIC PURPOSES
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/31/2012
84NYXSTIMULATOR, ELECTRICAL, TRANSCUTANEOUS, WITH LIMTED OUTPUT, FOR AESTHETIC PURPOSES
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/31/2012
84NYXSTIMULATOR, ELECTRICAL, TRANSCUTANEOUS, WITH LIMTED OUTPUT, FOR AESTHETIC PURPOSES
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/31/2012
84NYXSTIMULATOR, ELECTRICAL, TRANSCUTANEOUS, WITH LIMTED OUTPUT, FOR AESTHETIC PURPOSES
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/31/2012
84NYXSTIMULATOR, ELECTRICAL, TRANSCUTANEOUS, WITH LIMTED OUTPUT, FOR AESTHETIC PURPOSES
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)
12/31/2012
89JFBTABLE, PHYSICAL THERAPY, MULTI FUNCTION
118NOT LISTED
341REGISTERED
Florida District Office (FLA-DO)
12/31/2012
74DWJSYSTEM, THERMAL REGULATING
118NOT LISTED
341REGISTERED
Florida District Office (FLA-DO)
12/31/2012
74DWJSYSTEM, THERMAL REGULATING
118NOT LISTED
341REGISTERED
Florida District Office (FLA-DO)
12/31/2012
74DWJSYSTEM, THERMAL REGULATING
118NOT LISTED
341REGISTERED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Kallum Beauty Care Products Co Ltd's FDA import refusal history?

Kallum Beauty Care Products Co Ltd (FEI: 3009829353) has 9 FDA import refusal record(s) in our database, spanning from 12/31/2012 to 12/31/2012.

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. Kallum Beauty Care Products Co Ltd's FEI number is 3009829353.

What types of violations has Kallum Beauty Care Products Co Ltd received?

Kallum Beauty Care Products Co Ltd 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 Kallum Beauty Care Products Co Ltd come from?

All FDA import refusal data for Kallum Beauty Care Products 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.