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Arcadant B.V.

⚠️ Moderate Risk

FEI: 3014054090 • Liskeard, Cornwall • UNITED KINGDOM

FEI

FEI Number

3014054090

📍

Location

Liskeard, Cornwall

🇬🇧
🏢

Address

Prince Albert House, Quimperle Way; Liskeard Business Park, Liskeard, Cornwall, United Kingdom

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
12/6/2018
Latest Refusal
12/6/2018
Earliest Refusal

Score Breakdown

Violation Severity
63.3×40%
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).

24801×

RXPERSONAL

The article appears to be a device which requires a prescription from your doctor.

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
12/6/2018
86LPLLENSES, SOFT CONTACT, DAILY WEAR
118NOT LISTED
2480RXPERSONAL
508NO 510(K)
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Arcadant B.V.'s FDA import refusal history?

Arcadant B.V. (FEI: 3014054090) has 1 FDA import refusal record(s) in our database, spanning from 12/6/2018 to 12/6/2018.

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. Arcadant B.V.'s FEI number is 3014054090.

What types of violations has Arcadant B.V. received?

Arcadant B.V. 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 Arcadant B.V. come from?

All FDA import refusal data for Arcadant B.V. 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.