FDA Investigator: Kimberly Lewandowski-Walker

- Kimberly Lewandowski-Walker first started conducting FDA inspections in 2002, with the last inspection in 2017. Over that time, Kimberly Lewandowski-Walker has conducted 280 inspections at 230 companies across 238 sites.

Get Kimberly Lewandowski-Walker's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.

Documents

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FDA 483 RAUMEDIC - MUENCHBERG, Helmbrechts | 2017

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 Zevex Incorporated (dba Moog Medical Medical Devices Group), Salt Lake City | 2017

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 Oscor Inc., Palm Harbor | 2017

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 Medtronic Vascular Galway DBA Medtronic Ireland, Galway | 2016

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 Roche Diagnostics GmbH, Mannheim | 2016

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 Astute Medical, Inc., San Diego | 2016

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 UniStrip Technologies, LLC, Charlotte | 2015

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 Medtronic Vascular Galway DBA Medtronic Ireland, Galway | 2014

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 Orifice Medical AB, Ystad | 2014

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

FDA 483 St Jude Medical Inc, Plano | 2014

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Kimberly Lewandowski-Walker
Medical Devices & Rad Health Form 483

Co-Investigators (58)