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Food Products Manufacturing using Microsoft Dynamics AX 2012
Device manufacturer nets two item 483 for CAPA system flaws.(Medical Devices): An article from: Inspection Monitor
5-item 483 to drug manufacturer for lack of control procedures and for contamination issues.(HUMAN DRUGS): An article from: Inspection Monitor
Device manufacturer slapped with 9-item 483 for failure to report corrective/removal actions.(MEDICAL DEVICES/ CROs): An article from: Inspection Monitor
Audit of medical device manufacturer yields warning letter, 4-item 483.(Medical Devices): An article from: Inspection Monitor
Device manufacturer cited for CAPAs and MDRs in 11-item 483.(MEDICAL DEVICES): An article from: Inspection Monitor
Flawed process controls and design procedures net 9-item 483 for device manufacturer.(MEDICAL DEVICES): An article from: Inspection Monitor
Device manufacturer written up for validation process procedures in 11-item 483.(MEDICAL DEVICES): An article from: Inspection Monitor
Heating up sales at the January National Housewares Show: NHMA product roundup. (tea and coffee related items exhibited at the show sponsored by the ... An article from: Tea & Coffee Trade Journal