Madhu Instruments Private Limited
⚠️ Moderate Risk
FEI: 3007317099 • New Delhi, Delhi • INDIA
FEI Number
3007317099
Location
New Delhi, Delhi
Country
INDIAAddress
A - 260 Okhla Industrial Area Phase 1'St Road, , New Delhi, Delhi, 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).
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/13/2024 | 86HRHTREPHINE, MANUAL, OPHTHALMIC | 290DE IMP GMP | Division of Southeast Imports (DSEI) |
| 6/4/2024 | 86NCEINJECTOR, CAPSULAR TENSION RING | Division of Southeast Imports (DSEI) | |
| 6/4/2024 | 86NCEINJECTOR, CAPSULAR TENSION RING | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 6/4/2024 | 86NCEINJECTOR, CAPSULAR TENSION RING | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 6/4/2024 | 86NCEINJECTOR, CAPSULAR TENSION RING | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 4/2/2024 | 86HNIRETRACTOR, OPHTHALMIC | Division of Southeast Imports (DSEI) | |
| 12/7/2023 | 86KYGDEVICE, IRRIGATION, OCULAR SURGERY | 290DE IMP GMP | Division of Southeast Imports (DSEI) |
| 10/12/2021 | 86HMXCANNULA, OPHTHALMIC | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 10/12/2021 | 86KYDSTRIP, SCHIRMER | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 10/12/2021 | 86HMXCANNULA, OPHTHALMIC | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 8/17/2020 | 86HMXCANNULA, OPHTHALMIC | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Madhu Instruments Private Limited's FDA import refusal history?
Madhu Instruments Private Limited (FEI: 3007317099) has 11 FDA import refusal record(s) in our database, spanning from 8/17/2020 to 6/13/2024.
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. Madhu Instruments Private Limited's FEI number is 3007317099.
What types of violations has Madhu Instruments Private Limited received?
Madhu Instruments Private Limited has been cited for 4 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 Madhu Instruments Private Limited come from?
All FDA import refusal data for Madhu Instruments Private Limited 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.