MELROSE SURGICAL & DENTAL MANUFACTURING CO.
⚠️ Moderate Risk
FEI: 3017138688 • Sialkot, Punjab • PAKISTAN
FEI Number
3017138688
Location
Sialkot, Punjab
Country
PAKISTANAddress
18-A Small Industrial Estate (S.I.E.), , Sialkot, Punjab, Pakistan
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
DE IMP GMP
The article is subject to refusal of admission pursuant to section 801(a)(1) in that it appears that the methods used in, or the facilities or controls used for, the manufacture of the device do not conform to the applicable requirements of section 520(f).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/8/2020 | 76EMHFORCEPS, RONGEUR, SURGICAL | 290DE IMP GMP | Division of Southeast Imports (DSEI) |
| 9/8/2020 | 76EMGFORCEPS, TOOTH EXTRACTOR, SURGICAL | 290DE IMP GMP | Division of Southeast Imports (DSEI) |
| 9/1/2020 | 76EJGFORCEPS, RUBBER DAM CLAMP | 290DE IMP GMP | Division of Southeast Imports (DSEI) |
| 9/1/2020 | 76EMHFORCEPS, RONGEUR, SURGICAL | 290DE IMP GMP | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is MELROSE SURGICAL & DENTAL MANUFACTURING CO.'s FDA import refusal history?
MELROSE SURGICAL & DENTAL MANUFACTURING CO. (FEI: 3017138688) has 4 FDA import refusal record(s) in our database, spanning from 9/1/2020 to 9/8/2020.
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. MELROSE SURGICAL & DENTAL MANUFACTURING CO.'s FEI number is 3017138688.
What types of violations has MELROSE SURGICAL & DENTAL MANUFACTURING CO. received?
MELROSE SURGICAL & DENTAL MANUFACTURING CO. 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 MELROSE SURGICAL & DENTAL MANUFACTURING CO. come from?
All FDA import refusal data for MELROSE SURGICAL & DENTAL MANUFACTURING CO. 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.