Centroteam Ceramic Factory
⚠️ Moderate Risk
FEI: 1000453797 • Dongguan, Guangdong • CHINA
FEI Number
1000453797
Location
Dongguan, Guangdong
Country
CHINAAddress
Heng-Yi Street Ta-Tang, No. 26 Liaobu, Dongguan, Guangdong, China
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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
Frequently Asked Questions
What is Centroteam Ceramic Factory's FDA import refusal history?
Centroteam Ceramic Factory (FEI: 1000453797) has 2 FDA import refusal record(s) in our database, spanning from 3/19/2002 to 3/19/2002.
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. Centroteam Ceramic Factory's FEI number is 1000453797.
What types of violations has Centroteam Ceramic Factory received?
Centroteam Ceramic 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 Centroteam Ceramic Factory come from?
All FDA import refusal data for Centroteam Ceramic 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.