FDA Investigator: Kathleen D. Culver

- Kathleen D. Culver first started conducting FDA inspections in 2000, with the last inspection in 2016. Over that time, Kathleen D. Culver has conducted 235 inspections at 161 companies across 163 sites.

Get Kathleen Culver'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 Thorn BioScience LLC, Louisville | 2015

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Kathleen D. Culver
Animal Drugs & Feed Form 483

FDA 483 Mw Encap Ltd., Livingston | 2014

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Kathleen D. Culver
Human Drug Form 483

FDA 483 Albany Molecular Research UK Ltd., Flintshire, Wales | 2014

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Kathleen D. Culver
Animal Drugs & Feed Form 483

FDA 483 John E Pappas MD, Lexington | 2014

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Kathleen D. Culver
Human Drug Form 483

FDA 483 Coldstream Laboratories Inc, Lexington | 2014

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Kathleen D. Culver
Human Drug Form 483

FDA 483 New Lexington Clinic PSC IRB, Lexington | 2014

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Kathleen D. Culver
Human Drug Form 483

FDA 483 Tibor Csoszi, Szolnok | 2014

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Kathleen D. Culver
Human Drug Form 483

FDA 483 PETNET Solutions, Inc., Louisville | 2013

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Kathleen D. Culver
Human Drug Form 483