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Homeccas Remarketing Limited

⚠️ Moderate Risk

FEI: 3010019540 • Xiamenxiamen • CHINA

FEI

FEI Number

3010019540

📍

Location

Xiamenxiamen

🇨🇳

Country

CHINA
🏢

Address

Rm 506n Xin Gang Long Gardensiming, , Xiamenxiamen, , China

Moderate Risk

FDA Import Risk Assessment

44.1
LowModerateHighCritical

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

Statistics

12
Total Refusals
3
Unique Violations
4/25/2014
Latest Refusal
2/26/2013
Earliest Refusal

Score Breakdown

Violation Severity
54.4×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
100.0×10%
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

11812×

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).

32806×

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.

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
4/25/2014
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
New York District Office (NYK-DO)
4/25/2014
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
New York District Office (NYK-DO)
4/25/2014
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
New York District Office (NYK-DO)
4/25/2014
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
New York District Office (NYK-DO)
4/25/2014
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
New York District Office (NYK-DO)
4/25/2014
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
New York District Office (NYK-DO)
5/1/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
New York District Office (NYK-DO)
5/1/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
New York District Office (NYK-DO)
5/1/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
New York District Office (NYK-DO)
3/20/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
New York District Office (NYK-DO)
3/20/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
New York District Office (NYK-DO)
2/26/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
New York District Office (NYK-DO)

Frequently Asked Questions

What is Homeccas Remarketing Limited's FDA import refusal history?

Homeccas Remarketing Limited (FEI: 3010019540) has 12 FDA import refusal record(s) in our database, spanning from 2/26/2013 to 4/25/2014.

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. Homeccas Remarketing Limited's FEI number is 3010019540.

What types of violations has Homeccas Remarketing Limited received?

Homeccas Remarketing Limited 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 Homeccas Remarketing Limited come from?

All FDA import refusal data for Homeccas Remarketing Limited 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.