Day

July 1, 1996
Walter Graphtek Germany 7/1/96 EEG devices 3. Failure to perform planned and periodic audits in accordance with written procedures by appropriately trained individuals not having direct responsibility for the matters being audited, as required by 21 CFR 820.20(b). For example, the following areas were identified as having not been audited under your internal quality assurance...
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62304, FDA, and Emerging Standards for Medical Device and HealthIT
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Dates:  February 4-6, 2020

QSS Software Validation
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Dates:  June 2-4, 2020

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