FDA Inspection 947992 — GlaxoSmithKline Biologicals Kft.

GlaxoSmithKline Biologicals Kft. — FEI 3008322822

The FDA completed an inspection of GlaxoSmithKline Biologicals Kft. on Oct 6, 2015 in Godollo. 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
Oct 6, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Godollo (Hungary)

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