Exclusive NSF Whitepaper: FDA Medical Device Inspections and Recalls
An In-Depth Look Into FDA Policies and the Procedures That Shape Them
This comprehensive whitepaper is an all-in-one resource that provides a behind-the-scenes look at how FDA medical device inspections are planned, conducted, and managed. It also offers a ten-step approach to establishing and executing an effective FDA Medical Device 483 response and outlines actionable steps which may be taken when navigating an FDA recall of a medical device.
FDA Medical Device Inspection and Recalls is a must-read for any person who designs, manufactures, fabricates, assembles, or processes a finished device. This detailed paper offers a multi-layered exploration of FDA inspection activities, actions, and procedures appropriate for addressing them and achieving regulatory compliance.
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