DR VAIDYA MADHURA A BHIDE
⚠️ Moderate Risk
FEI: 3027512669 • Aundh Pune • INDIA
FEI Number
3027512669
Location
Aundh Pune
Country
INDIAAddress
Ayurved Plaza Deepak De, , Aundh Pune, , 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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
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 |
|---|---|---|---|
| 7/28/2023 | 62GCB36FLUNIXIN (ANTI-INFLAMMATORY) | Division of Southeast Imports (DSEI) | |
| 7/28/2023 | 61XDB51LEVOCETIRIZINE DIHYDROCHLORIDE | Division of Southeast Imports (DSEI) | |
| 7/28/2023 | 56ECA81TETRACYCLINE HYDROCHLORIDE (TETRACYCLINES) | Division of Southeast Imports (DSEI) | |
| 7/28/2023 | 63HDA22SENNA (CATHARTIC) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is DR VAIDYA MADHURA A BHIDE's FDA import refusal history?
DR VAIDYA MADHURA A BHIDE (FEI: 3027512669) has 4 FDA import refusal record(s) in our database, spanning from 7/28/2023 to 7/28/2023.
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. DR VAIDYA MADHURA A BHIDE's FEI number is 3027512669.
What types of violations has DR VAIDYA MADHURA A BHIDE received?
DR VAIDYA MADHURA A BHIDE 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 DR VAIDYA MADHURA A BHIDE come from?
All FDA import refusal data for DR VAIDYA MADHURA A BHIDE 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.