Resource - Webinars
How to Address an FDA 483 Warning Letter
This webinar is intended to address when and how to address FDA warning letters for device deficiencies.
Speaker(s)
John Waters
Regulatory Compliance Officer
John Waters has worked in some regulatory capacity for most of his career. John has spent the last seven years in medical device-related endeavors and because of his first hand FDA experience, he understands Quality System Regulations from the Agency’s perspective. John’s extensive experience with FDA includes areas related to 510 (k) Submissions, Medical Device Reports (MDR reporting), FDA inspections, Warning letter resolution, Device classification and company classification, and many other areas.
CE Credited Event