S.N. Corporation
⚠️ Moderate Risk
FEI: 3007336656 • Ahmedabad, Gujarat • INDIA
FEI Number
3007336656
Location
Ahmedabad, Gujarat
Country
INDIAAddress
7 Yogi Complexdrive In, 4th Floor, Ahmedabad, Gujarat, 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
UNSAFE COL
The article appears to be a color additive for the purposes of coloring only in or on drugs or devices, and is unsafe within the meaning of Section 721(a).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/6/2009 | 65PIY02SILDENAFIL CITRATE (REGULATOR) | Cincinnati District Office (CIN-DO) | |
| 3/6/2009 | 66SIY51TADALAFIL | Cincinnati District Office (CIN-DO) | |
| 3/6/2009 | 65PIY02SILDENAFIL CITRATE (REGULATOR) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 3/6/2009 | 65PIY04VARDENAFIL | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is S.N. Corporation's FDA import refusal history?
S.N. Corporation (FEI: 3007336656) has 4 FDA import refusal record(s) in our database, spanning from 3/6/2009 to 3/6/2009.
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. S.N. Corporation's FEI number is 3007336656.
What types of violations has S.N. Corporation received?
S.N. Corporation has been cited for 2 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 S.N. Corporation come from?
All FDA import refusal data for S.N. Corporation 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.