FDA Investigator: Lequita M. Mayhew

- Lequita M. Mayhew first started conducting FDA inspections in 2002, with the last inspection in 2019. Over that time, Lequita M. Mayhew has conducted 186 inspections at 154 companies across 155 sites.

Get Lequita Mayhew'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 Vifor Pharma Ltd, Glattbrugg | 2019

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Lequita M. Mayhew
Human Drug Form 483

FDA 483 Marianne Brodmann, MD, Graz | 2019

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Lequita M. Mayhew
Medical Devices & Rad Health Form 483

FDA 483 Sagent Pharmaceuticals, Inc., Schaumburg | 2018

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Lequita M. Mayhew
Human Drug Form 483

FDA 483 Trinity Medical Center-IRB, Rock Island | 2018

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Lequita M. Mayhew
Medical Devices & Rad Health Form 483

FDA 483 Northwestern University IRB, Chicago | 2018

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Lequita M. Mayhew
Biologic Form 483