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 » Wound Care Technologies Gets Form 483 for Inadequate Inspection, Complaint, MDR Procedures
Wound Care Technologies Gets Form 483 for Inadequate Inspection, Complaint, MDR Procedures
Wound Care Technologies, a provider of wound therapy systems, received a Form 483 from the FDA for inadequate inspection procedures for incoming products, as well as for its handling of complaints and medical device reporting (MDR).