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Glaxosmithkline

⚠️ Moderate Risk

FEI: 3006137887 • Guatemala City • GUATEMALA

FEI

FEI Number

3006137887

📍

Location

Guatemala City

🇬🇹

Country

GUATEMALA
🏢

Address

9 Avenida 0-09 Zona 4, , Guatemala City, , Guatemala

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
4/2/2007
Latest Refusal
4/2/2007
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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).

271×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

Refusal History

DateProductViolationsDivision
4/2/2007
65RBR18SODIUM BICARBONATE (REPLENISHER)
118NOT LISTED
27DRUG GMPS
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Glaxosmithkline's FDA import refusal history?

Glaxosmithkline (FEI: 3006137887) has 1 FDA import refusal record(s) in our database, spanning from 4/2/2007 to 4/2/2007.

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's FEI number is 3006137887.

What types of violations has Glaxosmithkline received?

Glaxosmithkline 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 come from?

All FDA import refusal data for Glaxosmithkline 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.