10/14/2026
In Bali, I recently dove with a guide who had been diving for over 25 years.
We were both dive master certified. He’d held his certification for over 15 years. I’d held mine for about a year—a significant difference in experience.
“What’s one of the most important things you’ve learned in all your years of diving?” I asked.
His answer: approach every dive the same when it comes to the safety check.
You don’t skip the safety checks. You don’t take your gear for granted. The ocean has a different temperament every time you go in, and you never know what you’re going to get.
Twenty-five years of experience, and he treated the safety checklist like it was day one.
That’s exactly what great RA/QA professionals do every day.
They’re the ones who insist the CAPA gets a real root cause. They keep the design history file current, catching the change that needs documenting before it becomes the recall everyone has to explain.
From the outside, that can look like caution slowing things down.
It isn’t. It’s the safety check.
The problems in FDA warning letters rarely start with RA/QA not knowing better. They start when the checks get treated as optional because a launch date or a quarter-end mattered more. In one recent letter, a company’s risk analysis was still the 2020 version, even after a Class I recall.
My guide didn’t need a reason to do his checks. He needed a dive operator that never rushed him.
For the C-suite leaders here:
When your RA/QA leaders ask for more people or more time, do you hear a cost or an investment and a safety check?