FDA Inspection 847467 - Lonza Manufacturing LLC - September 06, 2013
FDA Inspection 847467 for Lonza Manufacturing LLC on September 06, 2013. Classification: Voluntary Action Indicated (VAI).
One-time purchase from the GKS catalog. Lifetime access in your library. Single documents and full company profiles available. All sales final.
FDA Inspection 847467 for Lonza Manufacturing LLC on September 06, 2013. Classification: Voluntary Action Indicated (VAI).
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Lonza Manufacturing LLCInspection Date
September 6, 2013
Product Type
Drugs
ID: 234f67ce-8e58-4d7e-aece-fc5faa8e7675
View on DashboardTransform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.
Try KeyPedia Today
Explore our real use cases and discover our features in depth.
Subscribe to our newsletter
Get the latest updates and insights delivered to your inbox