Chongqing Dazu Imp Exp Corp
✅ Low Risk
FEI: 3003031803 • Ningno • CHINA
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/5/2001 | 76EFWTOOTHBRUSH, MANUAL | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Chongqing Dazu Imp Exp Corp's FDA import refusal history?
Chongqing Dazu Imp Exp Corp (FEI: 3003031803) has 1 FDA import refusal record(s) in our database, spanning from 10/5/2001 to 10/5/2001.
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. Chongqing Dazu Imp Exp Corp's FEI number is 3003031803.
What types of violations has Chongqing Dazu Imp Exp Corp received?
Chongqing Dazu Imp Exp Corp 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 Chongqing Dazu Imp Exp Corp come from?
All FDA import refusal data for Chongqing Dazu Imp Exp Corp 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.