FDA Inspection 1074726 - Protech Leaded Eyewear - December 14, 2018
FDA Inspection 1074726 for Protech Leaded Eyewear on December 14, 2018. 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 1074726 for Protech Leaded Eyewear on December 14, 2018. Classification: Voluntary Action Indicated (VAI).
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Protech Leaded EyewearInspection Date
December 14, 2018
Product Type
Devices
ID: fa54162e-036a-4b18-bed2-88f98234f2ca
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