Alrahma Co For Imp Expt
✅ Low Risk
FEI: 3010201394 • Shenzhen • 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 |
|---|---|---|---|
| 2/4/2014 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | 118NOT LISTED | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is Alrahma Co For Imp Expt's FDA import refusal history?
Alrahma Co For Imp Expt (FEI: 3010201394) has 1 FDA import refusal record(s) in our database, spanning from 2/4/2014 to 2/4/2014.
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. Alrahma Co For Imp Expt's FEI number is 3010201394.
What types of violations has Alrahma Co For Imp Expt received?
Alrahma Co For Imp Expt 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 Alrahma Co For Imp Expt come from?
All FDA import refusal data for Alrahma Co For Imp Expt 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.