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RHOPOINT INSTRUMENTATION LTD

⚠️ Moderate Risk

FEI: 3020284407 • St Leonards On Sea • UNITED KINGDOM

FEI

FEI Number

3020284407

📍

Location

St Leonards On Sea

🇬🇧
🏢

Address

Rhopoint House, Enviro 21 Business Park, St Leonards On Sea, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

33.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
12/2/2021
Latest Refusal
12/2/2021
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
11.2×30%
Recency
3.8×20%
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

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

Refusal History

DateProductViolationsDivision
12/2/2021
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
47NON STD
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is RHOPOINT INSTRUMENTATION LTD's FDA import refusal history?

RHOPOINT INSTRUMENTATION LTD (FEI: 3020284407) has 1 FDA import refusal record(s) in our database, spanning from 12/2/2021 to 12/2/2021.

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. RHOPOINT INSTRUMENTATION LTD's FEI number is 3020284407.

What types of violations has RHOPOINT INSTRUMENTATION LTD received?

RHOPOINT INSTRUMENTATION 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 RHOPOINT INSTRUMENTATION LTD come from?

All FDA import refusal data for RHOPOINT INSTRUMENTATION 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.