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 » FDA Cites Unapproved Changes to ASP’s Device Sterilizer
FDA Cites Unapproved Changes to ASP’s Device Sterilizer
June 3, 2010
The FDA is clamping down on sterilization devices made by Johnson & Johnson (J&J) unit Advanced Sterilization Products (ASP) — just months after forcing Steris to recall its sterilizing system.