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Aq Plc

⚠️ Moderate Risk

FEI: 3004545420 • Annbank Apraidr • UNITED KINGDOM

FEI

FEI Number

3004545420

📍

Location

Annbank Apraidr

🇬🇧
🏢

Address

The Lodge Interkine, , Annbank Apraidr, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

29.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
6/18/2004
Latest Refusal
6/18/2004
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

Refusal History

DateProductViolationsDivision
6/18/2004
68YAJ02HORSES ANIMAL DRUGS N.E.C.
336INCONSPICU
New Orleans District Office (NOL-DO)
6/18/2004
68YAJ02HORSES ANIMAL DRUGS N.E.C.
16DIRECTIONS
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Aq Plc's FDA import refusal history?

Aq Plc (FEI: 3004545420) has 2 FDA import refusal record(s) in our database, spanning from 6/18/2004 to 6/18/2004.

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. Aq Plc's FEI number is 3004545420.

What types of violations has Aq Plc received?

Aq Plc 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 Aq Plc come from?

All FDA import refusal data for Aq Plc 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.