FDA Investigator: Michele L. Glendenning

- Michele L. Glendenning first started conducting FDA inspections in 2013, with the last inspection in 2024. Over that time, Michele L. Glendenning has conducted 95 inspections at 79 companies across 88 sites.

Get Michele Glendenning'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 Akorn, Decatur | May 2018

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Michele L. Glendenning
Animal Drugs & Feed Form 483

FDA 483 AbbVie Inc., North Chicago | 2024

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 RIO BIOFARMA BRASIL LTDA, Hortolandia | 2024

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Baston Do Brasil Produtos Quimicos Ltda, Palmeira | 2024

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Combe Laboratories, Inc., Rantoul | 2024

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Accugen Laboratories, Inc., Addison | 2024

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Novartis Manufacturing LLC, Indianapolis | 2023

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Jiangxi Qingfeng Pharmaceutical Co., Ltd., Ganzhou | 2023

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Jiangsu Anbison Pharmaceutical Co., Ltd., Taizhou | 2023

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Medline Industries Inc, Mundelein | 2023

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Michele L. Glendenning
Human Drugs Form 483

FDA 483 Hospira Australia Pty Ltd., Mulgrave | 2022

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Michele L. Glendenning
Human Drug Form 483

FDA 483 Parsolex GMP Center, West Lafayette | 2022

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Michele L. Glendenning
Human Drug Form 483

Co-Investigators (46)