LENSAR, Inc.September 21, 2022

FDA 483 - LENSAR, Inc. - September 21, 2022

FDA 483 for LENSAR, Inc. on September 21, 2022. Product: device. Access full analysis and detailed observations.

One-time purchase from the GKS catalog. Lifetime access in your library. Single documents and full company profiles available. All sales final.

Record Summary

FDA 483 for LENSAR, Inc. on September 21, 2022. Product: device. Access full analysis and detailed observations.

Get More Insights

Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.

1.5M+ regulatory data points

Real-time compliance monitoring

Interactive analytics dashboard

Looking for more records? Our platform provides access to thousands of similar regulatory documents with advanced search and filtering capabilities.

Record Information

Company

LENSAR, Inc.

Inspection Date

September 21, 2022

Product Type

device

Office

Office of Medical Device and Radiological Health Division II

People

Natasha R. Johnson

ID: 05f0f77d-b74b-49ac-93f5-f62f559cc1e5

View on Dashboard

Transform 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