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FDA Inspection
•SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals)•July 5, 2019

SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals) – FDA Inspection, Jul 5, 2019

Record Details

This FDA Inspection record concerns SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals), with an inspection on July 5, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals)
Inspection Date
July 5, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Gene D. Arcy
View Company Profile

ID · 63db143a-b785-4875-96d0-efc0ded378e0

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1101506
FDA center
Biologics
Project area
Vaccines and Allergenic Products

Other FDA inspections of SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals)

6
DateClassificationOfficeProject area
March 15, 2024VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
September 20, 2022VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 27, 2017VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 22, 2011VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
May 24, 2010VAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
View all 6 other inspections on the company page
Other documents for SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals)
  • FDA Inspection 1233707 - 2024-03-15
  • FDA Inspection 1181891 - 2022-09-20
  • FDA Inspection 1019795 - 2017-06-27
  • FDA Inspection 736162 - 2011-06-22
  • FDA Inspection 668686 - 2010-05-24

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