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 » Lax Quality Control Operations Seen at Surgical Instrument Maker Genicon
Lax Quality Control Operations Seen at Surgical Instrument Maker Genicon
Devicemaker Genicon failed to provide adequate resources for quality control operations to ensure that devices were designed and produced according to FDA regulations, according to a 15-item Form 483 the firm received following an inspection of its Winter Park, Florida facility.
To View This Article:
Login
Subscribe To International Devices & Diagnostics Monitor