FDA Inspection 782611 - Mesa Laboratories, Inc., Bozeman Manufacturing Facility - May 11, 2012
FDA Inspection 782611 for Mesa Laboratories, Inc., Bozeman Manufacturing Facility on May 11, 2012. 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 782611 for Mesa Laboratories, Inc., Bozeman Manufacturing Facility on May 11, 2012. Classification: Voluntary Action Indicated (VAI).
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Inspection Date
May 11, 2012
Product Type
Devices
ID: f9ec1122-85e2-4eaf-baf1-b8de067834be
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