9.4 - Records and Reports - Quality Records micro lab Each person involved in manufacturing

Each person involved in manufacturing

and investigate if this may result in a risk of illness or injury

You must not reprocess a rejected dietary supplement or treat or provide an in-process adjustment to a component

composition

or storing dietary supplements

9.4 - Records and Reports - Quality Records micro lab Each person involved in manufacturingQuality records must be maintained for one year after expiry of the last batch implicated, including but not limited to batch disposition decisions, investigations into non conformances, OOS investigations, change controls, CAPA, returns, complaints, recalls, pest control, internal audits, supplier audits, and records of all training and qualifications