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Glaxosmithkline Pharmaceuticals

⚠️ Moderate Risk

FEI: 3003215515 • Harlow, Essex • UNITED KINGDOM

FEI

FEI Number

3003215515

📍

Location

Harlow, Essex

🇬🇧
🏢

Address

Science Park South, Third Avenue, Harlow, Essex, United Kingdom

Moderate Risk

FDA Import Risk Assessment

36.2
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
8/23/2011
Latest Refusal
7/30/2003
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
2.5×10%
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

752×

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).

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).

Refusal History

DateProductViolationsDivision
8/23/2011
61MIA38LAMOTRIGINE (ANTI-CONVULSANT)
118NOT LISTED
75UNAPPROVED
New Orleans District Office (NOL-DO)
7/30/2003
66VIS99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Philadelphia District Office (PHI-DO)

Frequently Asked Questions

What is Glaxosmithkline Pharmaceuticals's FDA import refusal history?

Glaxosmithkline Pharmaceuticals (FEI: 3003215515) has 2 FDA import refusal record(s) in our database, spanning from 7/30/2003 to 8/23/2011.

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. Glaxosmithkline Pharmaceuticals's FEI number is 3003215515.

What types of violations has Glaxosmithkline Pharmaceuticals received?

Glaxosmithkline Pharmaceuticals 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 Glaxosmithkline Pharmaceuticals come from?

All FDA import refusal data for Glaxosmithkline Pharmaceuticals 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.