FDA Inspection 1193493 — GlaxoSmithKline Biologicals

GlaxoSmithKline Biologicals — FEI 3016007176

The FDA completed an inspection of GlaxoSmithKline Biologicals on Nov 8, 2022 in Singapore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 8, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Singapore (Singapore)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.