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Morgan Innovation & Technology Ltd

⚠️ Moderate Risk

FEI: 3003255510 • Petersfield, Hampshire • UNITED KINGDOM

FEI

FEI Number

3003255510

📍

Location

Petersfield, Hampshire

🇬🇧
🏢

Address

Unit 17, Petersfield Business Park; Bedford Road, Petersfield, Hampshire, United Kingdom

Moderate Risk

FDA Import Risk Assessment

36.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
9/16/2011
Latest Refusal
9/16/2011
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
9/16/2011
87NBNGENERATOR, SHOCK-WAVE, (FOR PAIN RELIEF)
237NO PMA
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Morgan Innovation & Technology Ltd's FDA import refusal history?

Morgan Innovation & Technology Ltd (FEI: 3003255510) has 1 FDA import refusal record(s) in our database, spanning from 9/16/2011 to 9/16/2011.

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. Morgan Innovation & Technology Ltd's FEI number is 3003255510.

What types of violations has Morgan Innovation & Technology Ltd received?

Morgan Innovation & Technology Ltd 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 Morgan Innovation & Technology Ltd come from?

All FDA import refusal data for Morgan Innovation & Technology Ltd 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.