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FDA Inspection
•GSK LLC (GlaxoSmithKline)•November 1, 2012

GSK LLC (GlaxoSmithKline) – FDA Inspection, Nov 1, 2012

Record Details

This FDA Inspection record concerns GSK LLC (GlaxoSmithKline), with an inspection on November 1, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
GSK LLC (GlaxoSmithKline)
Inspection Date
November 1, 2012
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 6a59303c-a690-4300-8bae-39abb1bffe78

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
805603
FDA center
Human Drugs
Project area
Bioresearch Monitoring

Other FDA inspections of GSK LLC (GlaxoSmithKline)

8
DateClassificationOfficeProject area
August 19, 2026Not classifiedPhiladelphia District Office
October 21, 2025Not classifiedPhiladelphia District Office
November 22, 2024NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
October 24, 2022NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
August 12, 2022NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
View all 8 other inspections on the company page
Other documents for GSK LLC (GlaxoSmithKline)
  • FDA Inspection 1318026 - 2026-08-19
  • FDA Inspection 1269601 - 2025-10-21
  • FDA Inspection 1253764 - 2024-11-22
  • FDA Inspection 1187325 - 2022-10-24
  • FDA Inspection 1180594 - 2022-08-12

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