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Guide to Inspections of Medical Device Manufacturers 

December 1997 
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GUIDE TO INSPECTIONS OF

MEDICAL DEVICE MANUFACTURERS

December 1997

 
 

The Division of Emergency and Investigational Operations  
Office of Regional Operations  
Office of Regulatory Affairs  
U.S. Food & Drug Administration  

nbsp;Note:  this document is reference materials for investigators and other FDA personnel.  This Document does not bind FDA, and does not confer any rights, privileges, benifits, or immunities for  or on any personnel.

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