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FDA Inspection
•GlaxoSmithKline, LLC.•March 7, 2025

GlaxoSmithKline, LLC. – FDA Inspection, Mar 7, 2025

Record Details

This FDA Inspection record concerns GlaxoSmithKline, LLC., with an inspection on March 7, 2025, issued by the Philadelphia District Office, covering human drugs.

Company
GlaxoSmithKline, LLC.
Inspection Date
March 7, 2025
Product Type
Human Drugs
Office
Philadelphia District Office
People
  • Olumide A. Martins (Issuing Officer)
  • Shadia Zaman (Issuing Officer)
View Company Profile

ID · b8f525fd-c7f3-4be7-96cb-3b6521628f55

Inspection Facts

Inspection number
1274978
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of GlaxoSmithKline, LLC.

6
DateClassificationOfficeProject area
July 15, 2026Not classifiedPhiladelphia District Office
September 25, 2024Not classifiedPhiladelphia District Office
June 20, 2023NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 26, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 8, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for GlaxoSmithKline, LLC.
  • FDA Inspection 1332910 - 2026-07-15
  • FDA Inspection 1261906 - 2024-09-25
  • FDA Inspection 1211050 - 2023-06-20
  • FDA Inspection 1043309 - 2018-01-26
  • FDA Inspection 927643 - 2015-05-08

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