ImportRefusal LogoImportRefusal

Kenex

⚠️ Moderate Risk

FEI: 3002992599 • Essex • UNITED KINGDOM

FEI

FEI Number

3002992599

📍

Location

Essex

🇬🇧
🏢

Address

24 Burrill Mill, , Essex, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
11/17/2001
Latest Refusal
11/17/2001
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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

1181×

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).

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
11/17/2001
90IXYHOLDER, RADIOGRAPHIC CASSETTE, WALL-MOUNTED
118NOT LISTED
47NON STD
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Kenex's FDA import refusal history?

Kenex (FEI: 3002992599) has 1 FDA import refusal record(s) in our database, spanning from 11/17/2001 to 11/17/2001.

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. Kenex's FEI number is 3002992599.

What types of violations has Kenex received?

Kenex has been cited for 2 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 Kenex come from?

All FDA import refusal data for Kenex 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.