Holden Medical Laboratories
⚠️ Moderate Risk
FEI: 3006585377 • Nashik • INDIA
FEI Number
3006585377
Location
Nashik
Country
INDIAAddress
C-35/36 M.I.D.Cmalegaon, Sinar, , Nashik, , 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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/23/2017 | 60WCA16MEBENDAZOLE (ANTHELMINTIC) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 1/12/2012 | 60WAA16MEBENDAZOLE (ANTHELMINTIC) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 1/12/2012 | 61WAJ04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 6/2/2010 | 62KAA08LOPERAMIDE HYDROCHLORIDE (ANTI-PERISTALTIC, ANTI-DIARRHEAL) | New York District Office (NYK-DO) | |
| 6/2/2010 | 61WAA47KETOCONAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC) | New York District Office (NYK-DO) | |
| 6/2/2010 | 61FAB33ERTHROMYCIN ETHYLCARBONATE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | New York District Office (NYK-DO) | |
| 6/2/2010 | 61FAB33ERTHROMYCIN ETHYLCARBONATE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | New York District Office (NYK-DO) | |
| 6/2/2010 | 63FCA06DIGOXIN (CARDIOTONIC) | New York District Office (NYK-DO) | |
| 6/2/2010 | 61WCA04CLOTRIMAZOLE (ANTI-FUNGAL) (NOT ANTIBIOTIC) | New York District Office (NYK-DO) | |
| 6/2/2010 | 64LCJ08BETAMETHASONE VALERATE (GLUCOCORTICOID) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Holden Medical Laboratories's FDA import refusal history?
Holden Medical Laboratories (FEI: 3006585377) has 10 FDA import refusal record(s) in our database, spanning from 6/2/2010 to 3/23/2017.
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. Holden Medical Laboratories's FEI number is 3006585377.
What types of violations has Holden Medical Laboratories received?
Holden Medical Laboratories 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 Holden Medical Laboratories come from?
All FDA import refusal data for Holden Medical Laboratories 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.