FDA Investigator: Melanie M. Walker

- Melanie M. Walker first started conducting FDA inspections in 2006, with the last inspection in 2024. Over that time, Melanie M. Walker has conducted 25 inspections at 18 companies across 20 sites.

Get Melanie 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 Patheon Manufacturing Services LLC, Greenville | 2024

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Melanie M. Walker
Human Drugs Form 483

FDA 483 Gilead Sciences Inc, La Verne | 2024

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Melanie M. Walker
Human Drugs Form 483

FDA 483 King Bio Inc., Asheville | 2018

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Melanie M. Walker
Animal Drugs & Feed Form 483

FDA 483 CryoLife, Inc., Kennesaw | 2012

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Melanie M. Walker
Biologic Form 483

FDA 483 Novocol Pharmaceutical of Canada, Cambridge | 2012

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Melanie M. Walker
Human Drug Form 483

FDA 483 WuXi AppTec Inc., Marietta | 2011

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Melanie M. Walker
Medical Devices & Rad Health Form 483

FDA 483 Bausch & Lomb Inc- Greenville Solutions Plant, Greenville | 2009

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Melanie M. Walker
Medical Devices & Rad Health Form 483

FDA 483 Neuro Tec, Inc., Kennesaw | 2008

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Melanie M. Walker
Biologic Form 483