Changyang Qingjiang Pengbo Development
⚠️ Moderate Risk
FEI: 3010700818 • Changyang City • CHINA
FEI Number
3010700818
Location
Changyang City
Country
CHINAAddress
No 168 Changyang Ave, , Changyang City, , 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
VETDRUGRES
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/22/2014 | 16XVT02CATFISH, AQUACULTURE, FRESH WATER | 2860VETDRUGRES | Florida District Office (FLA-DO) |
| 5/5/2014 | 16XVT02CATFISH, AQUACULTURE, FRESH WATER | 2860VETDRUGRES | Florida District Office (FLA-DO) |
| 4/30/2014 | 16XVT02CATFISH, AQUACULTURE, FRESH WATER | 2860VETDRUGRES | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Changyang Qingjiang Pengbo Development's FDA import refusal history?
Changyang Qingjiang Pengbo Development (FEI: 3010700818) has 3 FDA import refusal record(s) in our database, spanning from 4/30/2014 to 5/22/2014.
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. Changyang Qingjiang Pengbo Development's FEI number is 3010700818.
What types of violations has Changyang Qingjiang Pengbo Development received?
Changyang Qingjiang Pengbo Development 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 Changyang Qingjiang Pengbo Development come from?
All FDA import refusal data for Changyang Qingjiang Pengbo Development 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.