SUN PHARMA MEDISALES PVT LTD
⚠️ High Risk
FEI: 3013657250 • Baddi, Himachal Pradesh • INDIA
FEI Number
3013657250
Location
Baddi, Himachal Pradesh
Country
INDIAAddress
1335 - 1340 Kh No, Near Ep, Baddi, Himachal 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
Frequently Asked Questions
What is SUN PHARMA MEDISALES PVT LTD's FDA import refusal history?
SUN PHARMA MEDISALES PVT LTD (FEI: 3013657250) has 2 FDA import refusal record(s) in our database, spanning from 7/31/2020 to 9/18/2025.
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. SUN PHARMA MEDISALES PVT LTD's FEI number is 3013657250.
What types of violations has SUN PHARMA MEDISALES PVT LTD received?
SUN PHARMA MEDISALES PVT LTD 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 SUN PHARMA MEDISALES PVT LTD come from?
All FDA import refusal data for SUN PHARMA MEDISALES PVT LTD 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.