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 » Warning Letter to UK Devicemaker Provides 483 Response Breakdown
Warning Letter to UK Devicemaker Provides 483 Response Breakdown
January 25, 2013
An FDA warning letter issued to British devicemaker Central Surgical offers an unusually detailed look at why the company’s Form 483 response was deemed insufficient.