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 » Deerfield Imaging Fails to Document CAPAs for X-Ray
The item has been added to your shopping cart.
Deerfield Imaging Fails to Document CAPAs for X-Ray
Failure to document corrective and preventive action (CAPA) activities related to its x-ray equipment landed Deerfied Imaging a Form 483 from the FDA following an inspection of its Minnetonka, Minnesota facility.