Maxtech Bath & Body Factory
⚠️ High Risk
FEI: 3003040139 • Shenzhen • CHINA
FEI Number
3003040139
Location
Shenzhen
Country
CHINAAddress
No. 12 Tong-Fu Ind., , Shenzhen, , China
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
HELD INSAN
The cosmetic appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/22/2011 | 53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 313HELD INSAN | Baltimore District Office (BLT-DO) |
| 11/22/2011 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 313HELD INSAN | Baltimore District Office (BLT-DO) |
| 11/22/2011 | 53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 313HELD INSAN | Baltimore District Office (BLT-DO) |
| 11/22/2011 | 53LD09SKIN FRESHENERS (SKIN CARE PREPARATIONS) | 313HELD INSAN | Baltimore District Office (BLT-DO) |
| 11/22/2011 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 313HELD INSAN | Baltimore District Office (BLT-DO) |
| 11/22/2011 | 53LD06MOISTURIZING (SKIN CARE PREPARATIONS) | 313HELD INSAN | Baltimore District Office (BLT-DO) |
Frequently Asked Questions
What is Maxtech Bath & Body Factory's FDA import refusal history?
Maxtech Bath & Body Factory (FEI: 3003040139) has 6 FDA import refusal record(s) in our database, spanning from 11/22/2011 to 11/22/2011.
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. Maxtech Bath & Body Factory's FEI number is 3003040139.
What types of violations has Maxtech Bath & Body Factory received?
Maxtech Bath & Body Factory 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 Maxtech Bath & Body Factory come from?
All FDA import refusal data for Maxtech Bath & Body Factory 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.