FDA Investigator: Burnell M. Henry

- Burnell M. Henry first started conducting FDA inspections in 2006, with the last inspection in 2024. Over that time, Burnell M. Henry has conducted 162 inspections at 121 companies across 134 sites.

Get Burnell Henry'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 LFB USA, Inc., Charlton | 2024

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Burnell M. Henry
Biologics Form 483

FDA 483 Kedrion Biopharma Inc., Melville | 2024

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Burnell M. Henry
Biologics Form 483

FDA 483 Pfizer Manufacturing Austria GmbH, Orth An Der Donau | 2023

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Burnell M. Henry
Biologics Form 483

FDA 483 Sanofi Pasteur, Marcy-L'Etoile | 2023

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Burnell M. Henry
Biologics Form 483

FDA 483 Pfizer Manufacturing Austria GmbH, Orth An Der Donau | 2022

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Burnell M. Henry
Biologic Form 483

FDA 483 Protherics UK Limited, Llandysul | 2022

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Burnell M. Henry
Biologic Form 483

FDA 483 MedImmune U.K. Limited, Liverpool | 2022

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Burnell M. Henry
Biologic Form 483

FDA 483 Corixa Corporation, Marietta | 2022

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Burnell M. Henry
Biologic Form 483

FDA 483 ADMA Biologics, Inc, Boca Raton | 2021

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Burnell M. Henry
Biologic Form 483

FDA 483 New York Blood Center Inc, Long Island City | 2020

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Burnell M. Henry
Biologic Form 483

FDA 483 Alk-abello A/s, Horsholm | 2019

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Burnell M. Henry
Biologic Form 483

FDA 483 Baxter Manufacturing S.p.A., Rieti | 2019

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Burnell M. Henry
Biologic Form 483

FDA 483 Sanofi Pasteur Limited - Cannaught Campus, North York | 2019

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Burnell M. Henry
Biologic Form 483

FDA 483 Corixa Corporation, Marietta | 2019

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Burnell M. Henry
Biologic Form 483

Co-Investigators (60)