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: HMI Failed to Conduct Proper Quality System Audit
FDA: HMI Failed to Conduct Proper Quality System Audit
March 31, 2010
HMI Industries has been warned for GMP violations related to its air-filtration devices, including failure to conduct quality audits.