ARCADIA BIOTECHNOLOGY LTD
⚠️ Moderate Risk
FEI: 3013336664 • SHANGHAI • CHINA
FEI Number
3013336664
Location
SHANGHAI
Country
CHINAAddress
SUITE 901 BUILDING WENS, , SHANGHAI, , 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
UNSFDIETSP
The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/9/2017 | 54YCR99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 2120UNSFDIETSP | Division of Southeast Imports (DSEI) |
| 5/30/2017 | 54ABA90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 2120UNSFDIETSP | Division of Southeast Imports (DSEI) |
| 5/30/2017 | 54ABA90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 2120UNSFDIETSP | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is ARCADIA BIOTECHNOLOGY LTD's FDA import refusal history?
ARCADIA BIOTECHNOLOGY LTD (FEI: 3013336664) has 3 FDA import refusal record(s) in our database, spanning from 5/30/2017 to 6/9/2017.
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. ARCADIA BIOTECHNOLOGY LTD's FEI number is 3013336664.
What types of violations has ARCADIA BIOTECHNOLOGY LTD received?
ARCADIA BIOTECHNOLOGY LTD 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 ARCADIA BIOTECHNOLOGY LTD come from?
All FDA import refusal data for ARCADIA BIOTECHNOLOGY LTD 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.