How Reliable Is Your Supply Chain?
Find out if your facility is at fault for any of these top 483 observations.
It's crucial to make sure your facility is aware & prepared for an FDA pop up inspection.
The FDA can come in at anytime and inspect a facility. The purpose of the FROM 483 is to help communicate any observations of specific practices that may be at fault for violating the FD&C Act.
These observations can vary from manufacturing processes to quality control and are publicly available through the Freedom of Information Act. Which means… you guessed it, is accessible to anyone and everyone.
Download the list to find out what Top 483 observations you should keep an eye out for.
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