FDA Investigator: Rebecca K. Olin
- Rebecca K. Olin first started conducting FDA inspections in 2006, with the last inspection in 2011. Over that time, Rebecca K. Olin has conducted 12 inspections at 12 companies across 12 sites.
Get Rebecca Olin'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 GlaxoSmithKline Biologicals, Dresden | 2011
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Rebecca K. Olin
Biologic Form 483
FDA 483 Ajinomoto Althea, Inc., San Diego | 2011
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Rebecca K. Olin
Biologic Form 483
FDA 483 CAF-DAF scrl, Neder-over- Heembeek | 2010
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Rebecca K. Olin
Biologic Form 483
FDA 483 Baxter Healthcare Corporation, Thousand Oaks | 2009
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Rebecca K. Olin
Biologic Form 483
FDA 483 Novartis Vaccines And Diagnostics Srl, Sovicille | 2009
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Rebecca K. Olin
Biologic Form 483
FDA 483 Baxter Manufacturing S.p.A., Rieti | 2008
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Rebecca K. Olin
Biologic Form 483
FDA 483 Merck Sharpe & Dohme Corp, West Point | 2008
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Rebecca K. Olin
Biologic Form 483
FDA 483 Glaxo Smithkline - Rixensart, Rixensart | 2007
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Rebecca K. Olin
Biologic Form 483
FDA 483 Sanofi Pasteur Inc., Swiftwater | 2006
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Rebecca K. Olin
Biologic Form 483
FDA 483 Baxter Pharmaceutical Solutions, LLC, Bloomington | 2006
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Rebecca K. Olin
Biologic Form 483
FDA 483 Octapharma AB, Stockholm | 2006
Out-of-stock
Rebecca K. Olin
Biologic Form 483