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 » API Maker Handed Form 483 After Failed Lab Controls and Repeat Observations
API Maker Handed Form 483 After Failed Lab Controls and Repeat Observations
Srikem Laboratories, an India-based active pharmaceutical ingredient manufacturer has been hit with a Form 483 after an inspection showed a number of repeat observations. The firm failed to meet established specifications, laboratory control procedures and equipment failures.