ImportRefusal LogoImportRefusal

AIR LIQUIDE HEALTHCARE NEDERLAND

⚠️ Moderate Risk

FEI: 3021499393 • Lelystad, Flevoland • NETHERLANDS

FEI

FEI Number

3021499393

📍

Location

Lelystad, Flevoland

🇳🇱
🏢

Address

Archimedeslaan 11, , Lelystad, Flevoland, Netherlands

Moderate Risk

FDA Import Risk Assessment

31.5
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
11/9/2022
Latest Refusal
11/9/2022
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
11.2×30%
Recency
22.5×20%
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).

32801×

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.

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
11/9/2022
75QCCINSULIN PUMP THERAPY ADJUSTMENT CALCULATOR FOR HEALTHCARE PROFESSIONALS
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is AIR LIQUIDE HEALTHCARE NEDERLAND's FDA import refusal history?

AIR LIQUIDE HEALTHCARE NEDERLAND (FEI: 3021499393) has 1 FDA import refusal record(s) in our database, spanning from 11/9/2022 to 11/9/2022.

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. AIR LIQUIDE HEALTHCARE NEDERLAND's FEI number is 3021499393.

What types of violations has AIR LIQUIDE HEALTHCARE NEDERLAND received?

AIR LIQUIDE HEALTHCARE NEDERLAND has been cited for 3 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 AIR LIQUIDE HEALTHCARE NEDERLAND come from?

All FDA import refusal data for AIR LIQUIDE HEALTHCARE NEDERLAND 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.