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 Issues 483 to Impax’s Troubled Hayward Plant
FDA Issues 483 to Impax’s Troubled Hayward Plant
March 12, 2013
Impax has been hit with another setback at its Hayward production facility as an FDA re-inspection resulted in a Form 483 for failing to meet quality standards.