Wheelchair Lift Firm Warned on CAPA, Complaint Handling

A bevvy of concerns about complaint handling and inventory led to an FDA warning letter for wheelchair-lift maker ThyssenKrupp Access Manufacturing. The letter — issued by the FDA’s Chicago district office on March 27 and posted online April 10 — follows a Nov. 8-10, 2011, inspection of the company’s Grandview, Mo., plant and issuance of a Form 483.
Devices & Diagnostics Letter