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 » Tyco Devices Misbranded, Deviate From cGMP Regulations, FDA Says
Tyco Devices Misbranded, Deviate From cGMP Regulations, FDA Says
November 3, 2005
Tyco Healthcare has received an FDA warning letter alleging the company's Mansfield, Mass., facility deviates from cGMP requirements.