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UNITED HAYEK INDUSTRIES MANUFACTURING LTD

⚠️ Moderate Risk

FEI: 3008808130 • London • UNITED KINGDOM

FEI

FEI Number

3008808130

📍

Location

London

🇬🇧
🏢

Address

10 Downage, , London, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

38.7
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
3/21/2025
Latest Refusal
4/25/2023
Earliest Refusal

Score Breakdown

Violation Severity
46.7×40%
Refusal Volume
17.7×30%
Recency
68.5×20%
Frequency
10.5×10%
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

32802×

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.

3412×

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).

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).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
3/21/2025
73BYTVENTILATOR, EXTERNAL BODY, NEGATIVE PRESSURE, ADULT (CUIRASS)
3280FRNMFGREG
341REGISTERED
Division of Southeast Imports (DSEI)
4/25/2023
73BYTVENTILATOR, EXTERNAL BODY, NEGATIVE PRESSURE, ADULT (CUIRASS)
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is UNITED HAYEK INDUSTRIES MANUFACTURING LTD's FDA import refusal history?

UNITED HAYEK INDUSTRIES MANUFACTURING LTD (FEI: 3008808130) has 2 FDA import refusal record(s) in our database, spanning from 4/25/2023 to 3/21/2025.

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. UNITED HAYEK INDUSTRIES MANUFACTURING LTD's FEI number is 3008808130.

What types of violations has UNITED HAYEK INDUSTRIES MANUFACTURING LTD received?

UNITED HAYEK INDUSTRIES MANUFACTURING LTD 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 UNITED HAYEK INDUSTRIES MANUFACTURING LTD come from?

All FDA import refusal data for UNITED HAYEK INDUSTRIES MANUFACTURING 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.