FDA Investigator: Merideth K. Rose

- Merideth K. Rose first started conducting FDA inspections in 2007, with the last inspection in 2012. Over that time, Merideth K. Rose has conducted 39 inspections at 37 companies across 37 sites.

Get Merideth Rose'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 Teva Pharmaceuticals Fine Chemicals S.r. i, Villanterio (PV) | 2012

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Merideth K. Rose
Human Drug Form 483

FDA 483 Union Quimico Farmaceutica, S.A. (Uquifa), Llica de Vail, Barcelona | 2012

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Merideth K. Rose
Human Drug Form 483

FDA 483 3CPM Company, Inc., Towson | 2011

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Merideth K. Rose
Medical Devices & Rad Health Form 483

FDA 483 Aphena Pharma Solutions-Maryland LLC, Easton | 2011

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Merideth K. Rose
Foods & Cosmetic Form 483

FDA 483 Cangene bioPharma, Inc., Baltimore | 2010

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Merideth K. Rose
Biologic Form 483

FDA 483 Guest Services, Inc., Jessup | 2010

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Merideth K. Rose
Foods & Cosmetic Form 483

FDA 483 Marcal Medical, Millersville | 2010

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Merideth K. Rose
Medical Devices & Rad Health Form 483

FDA 483 Sleep Solutions, Inc., Glen Burnie | 2010

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Merideth K. Rose
Medical Devices & Rad Health Form 483

FDA 483 3CPM Company, Inc., Towson | 2009

Out-of-stock
Merideth K. Rose
Medical Devices & Rad Health Form 483