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Wydia (HK) Limited

⚠️ Moderate Risk

FEI: 3013135195 • Hong Kong • CHINA

FEI

FEI Number

3013135195

📍

Location

Hong Kong

🇨🇳

Country

CHINA
🏢

Address

Rm 1205, 12/F Tai Sank Bank, Bldg 130-132 Des Voeux Rd, Hong Kong, , China

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
2/10/2017
Latest Refusal
2/10/2017
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

1971×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

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
2/10/2017
53CY99OTHER EYE MAKEUP PREPARATIONS, N.E.C.
197COSM COLOR
471CSTIC LBLG
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Wydia (HK) Limited's FDA import refusal history?

Wydia (HK) Limited (FEI: 3013135195) has 1 FDA import refusal record(s) in our database, spanning from 2/10/2017 to 2/10/2017.

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. Wydia (HK) Limited's FEI number is 3013135195.

What types of violations has Wydia (HK) Limited received?

Wydia (HK) Limited has been cited for 2 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 Wydia (HK) Limited come from?

All FDA import refusal data for Wydia (HK) 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.