FDA Investigator: Lori M. Newman

- Lori M. Newman first started conducting FDA inspections in 2021, with the last inspection in 2024. Over that time, Lori M. Newman has conducted 23 inspections at 18 companies across 21 sites.

Get Lori Newman'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 Denison Pharmaceuticals, LLC, Lincoln | 2024

Out-of-stock
Lori M. Newman
Human Drugs Form 483

FDA 483 Tom's of Maine, Inc., Sanford | 2024

Out-of-stock
Lori M. Newman
Human Drugs Form 483

FDA 483 Cipla Limited, Raigad | 2024

Out-of-stock
Lori M. Newman
Human Drugs Form 483

FDA 483 ZYDUS LIFESCIENCES LIMITED, Matoda | 2024

Out-of-stock
Lori M. Newman
Human Drugs Form 483

FDA 483 Freethink Technologies, Inc., Branford | 2024

Out-of-stock
Lori M. Newman
Human Drugs Form 483

FDA 483 AIRGAS USA, LLC., Salem | 2024

Out-of-stock
Lori M. Newman
Human Drugs Form 483

FDA 483 University Instrumentation Center at UNH, Durham | 2023

Out-of-stock
Lori M. Newman
Animal Drugs & Feeds Form 483

FDA 483 Lohxa, LLC, Worcester | 2023

Out-of-stock
Lori M. Newman
Human Drugs Form 483

FDA 483 Medical Technical Gases, Inc., N Billerica | 2022

Out-of-stock
Lori M. Newman
Human Drug Form 483

FDA 483 AIRGAS USA, LLC., Billerica | 2022

Out-of-stock
Lori M. Newman
Human Drug Form 483

FDA 483 Lohxa, LLC, Worcester | 2021

Out-of-stock
Lori M. Newman
Human Drug Form 483