FDA Inspection 1107165 — Lonza Biologics Tuas Pte Ltd

Lonza Biologics Tuas Pte Ltd — FEI 3009725845

The FDA completed an inspection of Lonza Biologics Tuas Pte Ltd on September 20, 2019 in Singapore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 20, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Singapore (Singapore)