FDA 483 - Airgas USA, LLC - June 21, 2023

Airgas USA, LLC in Lincoln Park, NJ, received a Form 483 with three observations following an inspection. The firm was cited for deficiencies in laboratory records, including a lack of complete data for non-compendial test methods. Additionally, the company failed to adhere to its own procedures for handling customer complaints, and batch records lacked proper identification for major equipment used in drug product manufacturing.