FDA Investigator: Linda F. Murphy

- Linda F. Murphy first started conducting FDA inspections in 2010, with the last inspection in 2020. Over that time, Linda F. Murphy has conducted 105 inspections at 103 companies across 103 sites.

Get Linda Murphy'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 UCLA Biomedical Cyclotron, Los Angeles | 2020

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Linda F. Murphy
Human Drug Form 483

FDA 483 Mylan Laboratories Limited, Speciality Formulation Facility, Bangalore | 2020

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Linda F. Murphy
Human Drug Form 483

FDA 483 Wintac Limited, Bangalore | 2020

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Linda F. Murphy
Human Drug Form 483

FDA 483 Morton Grove Pharmaceuticals, Inc., Morton Grove | 2019

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Linda F. Murphy
Human Drug Form 483

FDA 483 Teva Parenteral Medicines, Inc., Irvine | 2019

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Linda F. Murphy
Human Drug Form 483

FDA 483 Laboratoire Aguettant, Champagne | 2018

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Linda F. Murphy
Human Drug Form 483

FDA 483 FDC Limited, Aurangabad, Maharashtra State | 2018

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Linda F. Murphy
Human Drug Form 483

Co-Investigators (46)