FDA Inspection 925069 — Lonza Biologics Tuas Pte Ltd

Lonza Biologics Tuas Pte Ltd — FEI 3009725845

The FDA completed an inspection of Lonza Biologics Tuas Pte Ltd on Mar 10, 2015 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
Mar 10, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Singapore (Singapore)

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