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Molteno Ophthalmic Limited

⚠️ Moderate Risk

FEI: 3001227772 • Dunedin • NEW ZEALAND

FEI

FEI Number

3001227772

📍

Location

Dunedin

🇳🇿
🏢

Address

152 Frederick Street, North Dunedin, Dunedin, , New Zealand

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
1
Unique Violations
8/2/2010
Latest Refusal
8/2/2010
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

27801×

DEVICEGMPS

The article is subject to refusal of admission pursuant to Section 801(a)(1) in that the methods used in, or the facilities or controls used for, the manufacture, packing, storage, or installation of the device do not conform to the requirements of Section 520(f)(1) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) or a condition prescribed by an order under section 520(f)(2) of the FD&C Act.

Refusal History

DateProductViolationsDivision
8/2/2010
86KYFIMPLANT, EYE VALVE
2780DEVICEGMPS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Molteno Ophthalmic Limited's FDA import refusal history?

Molteno Ophthalmic Limited (FEI: 3001227772) has 1 FDA import refusal record(s) in our database, spanning from 8/2/2010 to 8/2/2010.

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. Molteno Ophthalmic Limited's FEI number is 3001227772.

What types of violations has Molteno Ophthalmic Limited received?

Molteno Ophthalmic Limited 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 Molteno Ophthalmic Limited come from?

All FDA import refusal data for Molteno Ophthalmic 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.