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AQ+ Plc Scotland

⚠️ Moderate Risk

FEI: 3005116373 • Angus • UNITED KINGDOM

FEI

FEI Number

3005116373

📍

Location

Angus

🇬🇧
🏢

Address

unknown, , Angus, , 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
6/28/2005
Latest Refusal
6/28/2005
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

162×

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.

3352×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

Refusal History

DateProductViolationsDivision
6/28/2005
55QA64PROPYLENE GLYCOL (PHARMACEUTIC NECESSITY - SOLVENT)
16DIRECTIONS
335LACKS N/C
New Orleans District Office (NOL-DO)
6/28/2005
68YBJ02HORSES ANIMAL DRUGS N.E.C.
16DIRECTIONS
335LACKS N/C
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is AQ+ Plc Scotland's FDA import refusal history?

AQ+ Plc Scotland (FEI: 3005116373) has 2 FDA import refusal record(s) in our database, spanning from 6/28/2005 to 6/28/2005.

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 Scotland's FEI number is 3005116373.

What types of violations has AQ+ Plc Scotland received?

AQ+ Plc Scotland 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 Scotland come from?

All FDA import refusal data for AQ+ Plc Scotland 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.