FDA 483 - Airgas USA, LLC - March 04, 2022

Airgas USA, LLC in Grand Junction, CO, was inspected for medical gas production and received a Form 483 with two observations. The firm failed to perform calibration on manifold gauges and gas analyzers at suitable intervals, leading to the distribution of unverified medical gas products. Additionally, the company did not maintain complete calibration records for laboratory gauges used in drug production.