Ciba Vision
⚠️ Moderate Risk
FEI: 3003552060 • Grosswallstadt • INDIA
FEI Number
3003552060
Location
Grosswallstadt
Country
INDIAAddress
Unknown Street, , Grosswallstadt, , India
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
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/1/2002 | 86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) | 2480RXPERSONAL | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is Ciba Vision's FDA import refusal history?
Ciba Vision (FEI: 3003552060) has 1 FDA import refusal record(s) in our database, spanning from 2/1/2002 to 2/1/2002.
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. Ciba Vision's FEI number is 3003552060.
What types of violations has Ciba Vision received?
Ciba Vision 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 Ciba Vision come from?
All FDA import refusal data for Ciba Vision 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.