FDA Investigator: Lisa M. Bellows

- Lisa M. Bellows first started conducting FDA inspections in 2001, with the last inspection in 2012. Over that time, Lisa M. Bellows has conducted 28 inspections at 24 companies across 25 sites.

Get Lisa Bellows's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.

Documents

Upon purchase, you will receive an email with a link to immediately download the documents.

FDA 483 Biochem Laboratories, Inc., Lyndhurst | 2012

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Mythen S.p.A., Corana (Pavia) | 2011

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Atral/Cipan, Castanheira Do Ribatejo | 2011

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Sunrise Pharmaceutical, Inc., Rahway | 2011

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Biochem Laboratories, Inc., Lyndhurst | 2011

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Omega Biological Laboratories Inc., Lyndhurst | 2011

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Lisa M. Bellows
Human Drug Form 483

FDA 483 KVK-Tech, Inc., Newtown | 2009

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Adhesives Research, Inc., Glen Rock | 2009

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Bayer Pharma AG, Berlin | 2008

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Teva Pharmaceuticals Fine Chemicals, Bulciago, Como | 2007

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Teva Pharmaceuticals Fine Chemicals S.r. i, Villanterio (PV) | 2007

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Olon S.p.A., Settimo Torinese | 2007

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Mutual Pharmaceutical Company, Inc., Philadelphia | 2005

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Eli Lilly And Company, Indianapolis | 2005

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Lisa M. Bellows
Human Drug Form 483

FDA 483 Asahi Kasei Finechem Corporation, Nobeoka | 2004

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Lisa M. Bellows
Human Drug Form 483