FDA Investigator: Brooke K. Higgins

- Brooke K. Higgins first started conducting FDA inspections in 2002, with the last inspection in 2014. Over that time, Brooke K. Higgins has conducted 222 inspections at 137 companies across 139 sites.

Get Brooke Higgins'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 Fresenius Medical Care de Mexico, Zapopan | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Elkton | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Barr Laboratories, Inc. (div. Of Teva), Forest | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Bell-More Laboratories Inc, Hampstead | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Afton Scientific, LLC, Charlottesville | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 United Therapeutics Corporation, Silver Spring | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Fareva Richmond, Inc., Henrico | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Teva Biopharmaceuticals USA, Rockville | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Precision Nuclear of Virginia, LLC, Salem | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 PETNET Solutions, Inc., Charlottesville | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 IBA Molecular, Sterling | 2013

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Brooke K. Higgins
Human Drug Form 483

FDA 483 Orion Corporation, Espoo | 2012

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Brooke K. Higgins
Animal Drugs & Feed Form 483

Co-Investigators (43)