9.4 - Records and Reports - Quality Records micro lab and investigate if this may

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

Complete internal audit checklist that ensures every aspect of dietary supplement GMP 21 CFR 111 has been implemented and can be used for periodic self-inspection to determine any gaps where corrective actions and preventative actions (CAPA) can be assigned and mitigated

Returned or reprocessed drug product shall be destroyed unless examination

or storing dietary supplements

9.4 - Records and Reports - Quality Records micro lab and investigate if this mayQuality 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