FDA Investigator: Michael E. Maselli

- Michael E. Maselli first started conducting FDA inspections in 2002, with the last inspection in 2023. Over that time, Michael E. Maselli has conducted 62 inspections at 60 companies across 61 sites.

Get Michael Maselli'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 Rohto Pharmaceutical Co., Ltd. (Ueno Plant), Iga | 2023

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Michael E. Maselli
Human Drugs Form 483

FDA 483 Toyobo Co. Ltd., Otsu | 2023

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Michael E. Maselli
Human Drugs Form 483

FDA 483 Isotopia Molecular Imaging Ltd (Soreq Site), Yavne | 2019

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Michael E. Maselli
Human Drug Form 483

FDA 483 Sage Products Inc, Cary | 2016

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Michael E. Maselli
Medical Devices & Rad Health Form 483

FDA 483 Hikma Farmaceutica, (Portugal) S.A., Terrugem Snt | 2015

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Michael E. Maselli
Human Drug Form 483

FDA 483 Recipharm Monts, Monts | 2015

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Michael E. Maselli
Human Drug Form 483

FDA 483 Genzyme Flanders N.v., Geel | 2013

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Michael E. Maselli
Human Drug Form 483

FDA 483 Merck Serono Aubonne, Aubonne | 2013

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Michael E. Maselli
Human Drug Form 483

FDA 483 OSO BioPharmaceuticals Manufacturing, LLC, Albuquerque | 2013

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Michael E. Maselli
Human Drug Form 483

FDA 483 Uman Pharma, Inc., Candiac | 2012

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Michael E. Maselli
Human Drug Form 483

FDA 483 AlloSource Inc, Centennial | 2012

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Michael E. Maselli
Biologic Form 483

FDA 483 Glaxo Operations UK Limited, Ware | 2012

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Michael E. Maselli
Human Drug Form 483

FDA 483 Laleham Healthcare Limited, Alton | 2012

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Michael E. Maselli
Human Drug Form 483