FDA Investigator: Susan T. Hadman

- Susan T. Hadman first started conducting FDA inspections in 2001, with the last inspection in 2024. Over that time, Susan T. Hadman has conducted 57 inspections at 54 companies across 56 sites.

Get Susan Hadman'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 NerPharMa S.r.l., Nerviano | 2023

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Susan T. Hadman
Human Drugs Form 483

FDA 483 Industrias Farmaceuticas Almirall S.A., Sant Andreu De La Barca | 2023

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Susan T. Hadman
Human Drugs Form 483

FDA 483 Merz Pharma GmbH & Co., KGaA, Dessau-Rosslau | 2019

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Susan T. Hadman
Human Drug Form 483

FDA 483 Liof Pharma S.L., Vitoria | 2019

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Susan T. Hadman
Human Drug Form 483

FDA 483 Goodwin Biotechnology, Inc., Plantation | 2019

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Susan T. Hadman
Human Drug Form 483

FDA 483 Sandoz GmbH, Kundl | 2018

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Susan T. Hadman
Human Drug Form 483

FDA 483 Pascal Co Inc, Bellevue | 2018

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Susan T. Hadman
Human Drug Form 483

FDA 483 Amgen Technology Ireland UC, Dun Laoghaire | 2017

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Susan T. Hadman
Human Drug Form 483

FDA 483 Laboratorio Reig Jofre S.A., Sant Joan Despi | 2015

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Susan T. Hadman
Human Drug Form 483

FDA 483 Laboratorio Reig Jofre S.A., Toledo | 2015

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Susan T. Hadman
Human Drug Form 483