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Carrie Kehoe

⚠️ Moderate Risk

FEI: 3003851542 • Mullingar, Co. WESTMEATH • IRELAND

FEI

FEI Number

3003851542

📍

Location

Mullingar, Co. WESTMEATH

🇮🇪

Country

IRELAND
🏢

Address

30 Dominick Street, , Mullingar, Co. WESTMEATH, Ireland

Moderate Risk

FDA Import Risk Assessment

39.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
12/13/2002
Latest Refusal
12/13/2002
Earliest Refusal

Score Breakdown

Violation Severity
80.0×40%
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

3311×

DR QUALITC

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the drug appears to be represented as not being recognized in an official compendium and appears its strength differs from or its quality or purity falls below, that which it purports or is represented to possess.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
12/13/2002
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
331DR QUALITC
New Orleans District Office (NOL-DO)
12/13/2002
66VCA99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Carrie Kehoe's FDA import refusal history?

Carrie Kehoe (FEI: 3003851542) has 2 FDA import refusal record(s) in our database, spanning from 12/13/2002 to 12/13/2002.

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. Carrie Kehoe's FEI number is 3003851542.

What types of violations has Carrie Kehoe received?

Carrie Kehoe 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 Carrie Kehoe come from?

All FDA import refusal data for Carrie Kehoe 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.