Deepali
⚠️ High Risk
FEI: 3007803880 • Ghaziabad, Uttar Pradesh • INDIA
FEI Number
3007803880
Location
Ghaziabad, Uttar Pradesh
Country
INDIAAddress
I - 503 Jai Puria Sun Rise Greens Ahinsa, , Ghaziabad, Uttar Pradesh, India
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/13/2009 | 61LCA38CLOPIDOGREL BISULFATE (ANTI-COAGULANT) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 55YY99PHARMACEUTIC NECESSITIES AND CONTAINERS, N.E.C. | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 55YY99PHARMACEUTIC NECESSITIES AND CONTAINERS, N.E.C. | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 60LCA05ASPIRIN (ANALGESIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 64BCA48INDAPAMIDE (DIURETIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 61PCA26METFORMIN (ANTI-DIABETIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 61PCA31GLIMEPIRIDE (ANTI-DIABETIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 61XCA45CETIRIZINE HYDROCHLORIDE (ANTI-HISTAMINIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 10/13/2009 | 64BCA24FUROSEMIDE (DIURETIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Deepali's FDA import refusal history?
Deepali (FEI: 3007803880) has 9 FDA import refusal record(s) in our database, spanning from 10/13/2009 to 10/13/2009.
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. Deepali's FEI number is 3007803880.
What types of violations has Deepali received?
Deepali 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 Deepali come from?
All FDA import refusal data for Deepali 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.