ImportRefusal LogoImportRefusal

Ladycare Amenities Manufacturing Company Limited

✅ Low Risk

FEI: 3003214885 • Kowloon Bay, Kowloon • HONG KONG

FEI

FEI Number

3003214885

📍

Location

Kowloon Bay, Kowloon

🇭🇰

Country

HONG KONG
🏢

Address

Rm 2207-2211, 22/F, Telford House; 16 Wang Hoi Road, Kowloon Bay, Kowloon, Hong Kong

Low Risk

FDA Import Risk Assessment

20.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
10/20/2008
Latest Refusal
10/20/2008
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
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

4711×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

Refusal History

DateProductViolationsDivision
10/20/2008
53LD06MOISTURIZING (SKIN CARE PREPARATIONS)
471CSTIC LBLG
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ladycare Amenities Manufacturing Company Limited's FDA import refusal history?

Ladycare Amenities Manufacturing Company Limited (FEI: 3003214885) has 1 FDA import refusal record(s) in our database, spanning from 10/20/2008 to 10/20/2008.

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. Ladycare Amenities Manufacturing Company Limited's FEI number is 3003214885.

What types of violations has Ladycare Amenities Manufacturing Company Limited received?

Ladycare Amenities Manufacturing Company Limited has been cited for 1 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 Ladycare Amenities Manufacturing Company Limited come from?

All FDA import refusal data for Ladycare Amenities Manufacturing Company 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.