FDA Investigator: Kathleen R. Jones

- Kathleen R. Jones first started conducting FDA inspections in 2017, with the last inspection in 2023. Over that time, Kathleen R. Jones has conducted 14 inspections at 13 companies across 14 sites.

Get Kathleen Jones'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 Recipharm AB, Oeiras | 2023

Out-of-stock
Kathleen R. Jones
Biologics Form 483

FDA 483 Novo Nordisk US Bio Production Inc., West Lebanon | 2020

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Kathleen R. Jones
Biologic Form 483

FDA 483 Patheon Biologics B.V., Groningen | 2018

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Kathleen R. Jones
Human Drug Form 483

FDA 483 Boehringer Ingelheim Pharma Gmbh & Co Kg, Biberach an der Ris | 2017

Out-of-stock
Kathleen R. Jones
Human Drug Form 483