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» Public Workshop: Medical Device Quality System Regulation Educational Forum on Risk Management Through the Product Life Cycle
Public Workshop: Medical Device Quality System Regulation Educational Forum on Risk Management Through the Product Life Cycle
Document ID:
FDA-2009-N-0664-0133
Document Type:
Notice
Agency:
Food And Drug Administration
Topics:
No Topics associated with this document
Federal Register Number:
E9-31198
View Document:
Details Information
Document Subtype:
NM-Notice of Meeting
Received Date:
January 04 2010, at 09:04 AM Eastern Standard Time
Start-End Page:
391 - 391
Page Count:
1
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Public Workshop: Medical Device Quality System Regulation Educational Forum on Risk Management Through the Product Life Cycle
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