We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Wyeth’s Richmond Plant Slow to Alert on Batch Misfires: Form 483
Wyeth’s Richmond Plant Slow to Alert on Batch Misfires: Form 483
January 3, 2012
Wyeth’s Richmond, Va., plant failed to submit timely alerts for one or more distributed batches of drugs observed by customers as not up to specification, an FDA Form 483 states.