LIFESAN MEDICAL DEVICES INDIA PV
⚠️ High Risk
FEI: 3016831465 • Mumbai • 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 |
|---|---|---|---|
| 6/30/2025 | 66VDY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is LIFESAN MEDICAL DEVICES INDIA PV's FDA import refusal history?
LIFESAN MEDICAL DEVICES INDIA PV (FEI: 3016831465) has 1 FDA import refusal record(s) in our database, spanning from 6/30/2025 to 6/30/2025.
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. LIFESAN MEDICAL DEVICES INDIA PV's FEI number is 3016831465.
What types of violations has LIFESAN MEDICAL DEVICES INDIA PV received?
LIFESAN MEDICAL DEVICES INDIA PV 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 LIFESAN MEDICAL DEVICES INDIA PV come from?
All FDA import refusal data for LIFESAN MEDICAL DEVICES INDIA PV 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.