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 » Michigan Manufacturer Vertellus Hit With 483 for Quality and Other Violations
Michigan Manufacturer Vertellus Hit With 483 for Quality and Other Violations
Detroit-based drug manufacturer Vertellus received a Form 483 with 7 observations from an FDA inspection of its Zeeland, Mich. facility. The Mar. 25-April 9 inspection revealed problems across the facility’s quality, materials, and laboratory systems.