FDA Investigator Timothy G Philips

Timothy G Philips has conducted inspections on 13 sites in 4 countries as of 24 Jul 2018. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
13
Last Inspection Date:
24 Jul 2018
Investigator Role:
FDA Investigator
Redica ID:
100009356
Countries of Inspections:
United States of America, United Kingdom of Great Britain and Northern Ireland, Germany, Italy
FDA Investigators that have inspected at least one site in common with Timothy G Philips:
Aaron L Dunbar, Aimee J Edwin, Alison A Nicoli, Alison A Stone, Althea A Williams, Annabelle Crusan, D,VM, April L Brown, April L Young, Benjamin J Dastoli, Benjamin W Anderson, Billi Jom Johnson, Carolyn A Warren, Catherine J Laufmann, Christina L Bigham, Demetria L Lueneburg, Dolores Harper, Douglas W Atkins, Eric M Padgett, Evelyn Taha, Jaclyn N Munsch, James A Beaulieu, James D Planchon, Janis R Armedoriz, Jay V Jariwala, Jennifer S Ness, Jessica L Johnson, Jocelyn M Muggli, Joey C West, Joseph D Gong, Joseph M Edwin, Karen M Montgomery (KMM), Kellie L Thommes, RN, Kellie L Westerbuhr, Kimberly Lewandowski Walker, Kristy E Zuroski, Kyle J Mccracken, Laiza V Garcia, Marie A Fadden, Marissa S Henning, Marissa S Steinhagen, Mary A Millner, Maryam Tabatabaie, Melanie W Pishnery, Melissa I Michurski, Michael J Nerz, Nicole C Victoria, PhD, Norman Wong, Paul M Kawamoto, Ralph Jerndal, Rhonda L Mecl, Richard Jay Tucker, RS, Richard L Rutherford, Robert G Ruff, Rosanna M Goodrich, Ryan J Benedict, Shannon M Berg, Sharon L Matson, Stephen D Eich, Susan A Atcher, Susan M Atcher, Susan M Matthias, Tania E Vizcaino, Timothy R Marrs, Tony T Yang, Tyler R Courtney, Victor Spanioli, Wanda J Torres, William D Tingley, Yehualashet A Gessesse

Timothy G Philips's Documents

Publish Date Document Type Title
January, 2000 FDA 483 Boston Scientific Corporation - Form 483, 2000-01-14
January, 2007 FDA 483 Medtronic Neuromodulation - Form 483, 2007-01-24
January, 2007 EIR Medtronic Neuromodulation - EIR, 2007-01-24
June, 2006 FDA 483 Medtronic Neuromodulation - Form 483, 2006-06-22

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