FDA Inspection 994781 - Grifols Therapeutics LLC - October 21, 2016
FDA Inspection 994781 for Grifols Therapeutics LLC on October 21, 2016. 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 994781 for Grifols Therapeutics LLC on October 21, 2016. Classification: Voluntary Action Indicated (VAI).
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Grifols Therapeutics LLCInspection Date
October 21, 2016
Product Type
Biologics
ID: 9a41f385-bd40-454e-bfcf-1cf95a896584
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