FDA Inspection 857625 — Glaxo Wellcome S.A.

Glaxo Wellcome S.A. — FEI 3004195227

The FDA completed an inspection of Glaxo Wellcome S.A. on Sep 27, 2013 in Aranda De Duero. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 27, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Aranda De Duero (Spain)