4min 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

Is the Past Destined to Repeat Itself?

Mike Drew: I really wish that we worked in an industry where we wouldn't need the FDA telling us to do things. The top three reasons why companies get either 43 or warning letters are CAPA's design controls and complaints. If you're doing what you should do, maybe you don't need those regulatory requirements. Those are for people who aren't doing quite enough.

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