Glow World Instruments
⚠️ Moderate Risk
FEI: 3009630339 • Sialkot • PAKISTAN
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
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/2/2012 | 77KBNGAG, MOUTH | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 77KBNGAG, MOUTH | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 77KBNGAG, MOUTH | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 78KOEDILATOR, URETHRAL | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 78KOEDILATOR, URETHRAL | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 78KOEDILATOR, URETHRAL | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 78KOEDILATOR, URETHRAL | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 78KOEDILATOR, URETHRAL | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
| 8/2/2012 | 78KOEDILATOR, URETHRAL | 16DIRECTIONS | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Glow World Instruments's FDA import refusal history?
Glow World Instruments (FEI: 3009630339) has 9 FDA import refusal record(s) in our database, spanning from 8/2/2012 to 8/2/2012.
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. Glow World Instruments's FEI number is 3009630339.
What types of violations has Glow World Instruments received?
Glow World Instruments 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 Glow World Instruments come from?
All FDA import refusal data for Glow World Instruments 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.