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Technology Good manufacturing practice Form FDA 483 Center for Devices and Radiological Health Medical device Design controls Quality management system QSIT Title 21 of the Code of Federal Regulations Food and Drug Administration Medicine Health		Microsoft Word - 1- CP[removed]Coversheet February[removed]Final.doc Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 623,47 KB Share Document on Facebook

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