Actman Corporation
⚠️ Moderate Risk
FEI: 1000508791 • Taipei Hsien • TAIWAN
FEI Number
1000508791
Location
Taipei Hsien
Country
TAIWANAddress
3f., No. 11 Pao Hao Road, , Hsin Tein, Taipei Hsien, , Taiwan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/9/2001 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 475COSMETLBLG | New York District Office (NYK-DO) |
| 10/9/2001 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | 475COSMETLBLG | New York District Office (NYK-DO) |
| 10/9/2001 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | New York District Office (NYK-DO) | |
| 10/9/2001 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | New York District Office (NYK-DO) | |
| 10/9/2001 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | New York District Office (NYK-DO) | |
| 10/9/2001 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | New York District Office (NYK-DO) | |
| 10/9/2001 | 53CY03EYE SHADOW (EYE MAKEUP PREPARATIONS) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Actman Corporation's FDA import refusal history?
Actman Corporation (FEI: 1000508791) has 7 FDA import refusal record(s) in our database, spanning from 10/9/2001 to 10/9/2001.
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. Actman Corporation's FEI number is 1000508791.
What types of violations has Actman Corporation received?
Actman Corporation 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 Actman Corporation come from?
All FDA import refusal data for Actman Corporation 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.