FDA Inspection 1275331 — Glaxo Wellcome Manufacturing Pte Limited

Glaxo Wellcome Manufacturing Pte Limited — FEI 3002807079

The FDA completed an inspection of Glaxo Wellcome Manufacturing Pte Limited on Oct 13, 2023 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 13, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Singapore (Singapore)

Additional Details

Mutual Recognition Agreement (MRA)