FDA Investigator Susan M Atcher

Susan M Atcher has conducted inspections on 22 sites in 2 countries as of 16 Sep 2014. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
22
Last Inspection Date:
16 Sep 2014
Investigator Role:
FDA Investigation Participant
Redica ID:
100003883
Countries of Inspections:
United States of America, Canada
FDA Investigators that have inspected at least one site in common with Susan M Atcher:
Aaron L Dunbar, Aimee J Edwin, Albert L Nguyen, Alison A Nicoli, Alison A Stone, Althea A Williams, Ana M Placencia, Annabelle Crusan, D,VM, April L Brown, April L Young, Benjamin W Anderson, Billi Jom Johnson, Christina L Bigham, Demetria L Lueneburg, Dolores Harper, Douglas W Atkins, Gregory A Berg, James A Beaulieu, James R Fleckenstein, Janis R Armedoriz, Jay V Jariwala, Jennifer S Ness, Jessica L Johnson, Jocelyn M Muggli, Joey C West, Joseph D Gong, Joseph M Edwin, Kellie L Thommes, RN, Kellie L Westerbuhr, Kimberly Lewandowski Walker, Kyle J Mccracken, Lanita F Kelley, Lori S Lawless, Marie A Fadden, Marissa S Henning, Marissa S Steinhagen, Melissa I Michurski, Nicole C Victoria, PhD, Norman Wong, Paquita F Segarra, Ralph Jerndal, Ralph W Jemdal, Rhonda L Mecl, Ross J Grigsby, Scott A Golladay, Sharon L Matson, Susan A Atcher, Susan M Matthias, Timothy G Philips, Timothy R Marrs, Tony T Yang, Toyin B Oladimeji, Tyler R Courtney, Yehualashet A Gessesse, Yoon K Oh

Susan M Atcher's Documents

Publish Date Document Type Title
September, 2012 FDA 483 CareFusion 203, Inc. - Form 483, 2012-09-05
January, 2011 FDA 483 Medtronic Neuromodulation - Form 483, 2011-01-21
February, 2014 FDA 483 Verathon Medical - Form 483, 2014-02-14
October, 2011 EIR Lake Region Manufacturing, Inc - EIR, 2011-10-17
September, 2009 FDA 483 CareFusion 203, Inc. - Form 483, 2009-09-18
April, 2012 FDA 483 Boston Scientific Corporation - Form 483, 2012-04-16
September, 2010 FDA 483 Nonin Medical, Inc - Form 483, 2010-09-24
September, 2014 FDA 483 Penrad Technologies, Inc. - Form 483, 2014-09-19
April, 2011 FDA 483 St. Jude Medical Atrial Fibrillation - Form 483, 2011-10-26
July, 2011 FDA 483 Lifecore Biomedical, LLC - Form 483, 2011-08-29
February, 2014 EIR Verathon Medical - EIR, 2014-02-14
February, 2012 FDA 483 Boston Scientific Corporation - Form 483, 2012-04-19
April, 2014 EIR Smiths Medical ASD, Inc. - EIR, 2014-04-23
April, 2014 FDA 483 Smiths Medical ASD, Inc. - Form 483, 2014-04-23
June, 2010 EIR DentalEZ dba Ramvac Corporation - EIR, 2010-06-11
January, 2010 FDA 483 St. Jude Medical Atrial Fibrillation - Form 483, 2010-01-22
March, 2010 FDA 483 Nortech Systems, Inc. - Form 483, 2010-03-04
October, 2012 FDA 483 Dane Technologies - Form 483, 2012-10-17
December, 2008 FDA 483 St. Jude Medical Atrial Fibrillation - Form 483, 2008-12-19
April, 2010 FDA 483 Chitogen, Inc. - Form 483, 2010-04-12
July, 2010 FDA 483 PMT Corporation - Form 483, 2010-07-16
October, 2009 FDA 483 Medtronic Monitoring Inc. - Form 483, 2009-10-23
August, 2011 FDA 483 Medtronic Inc. - Form 483, 2011-08-24
July, 2013 FDA 483 NEOMETRICS, INC. - Form 483, 2013-07-03
December, 2008 FDA 483 Response St. Jude Medical Atrial Fibrillation - Form 483R, 2009-01-28

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