2min chapter

Global Medical Device Podcast powered by Greenlight Guru cover image

Most Common Problems Found During FDA Inspections in 2022

Global Medical Device Podcast powered by Greenlight Guru

CHAPTER

Most Common Reasons for 43s

Roxanne Jones: I've seen this in multiple companies, where you throw together some sort of risk management file for your design. She says the documents don't inform the design because they don't have to inform the design. "There's no mechanism to force that and maybe this goes to, you know, one of the main issues," she adds.

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