FDA Investigator: Robert G. Ruff

- Robert G. Ruff first started conducting FDA inspections in 2000, with the last inspection in 2010. Over that time, Robert G. Ruff has conducted 108 inspections at 77 companies across 78 sites.

Get Robert Ruff'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 Howmedica Osteonics Corp. d.b.a. Stryker Spine, Summit | 2010

Out-of-stock
Robert G. Ruff
Medical Devices & Rad Health Form 483

FDA 483 Mindray DS USA, Inc. dba Mindray North America, Mahwah | 2010

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Robert G. Ruff
Medical Devices & Rad Health Form 483

FDA 483 Maquet Datascope Corp - Cardiac Assist Division, Mahwah | 2010

Out-of-stock
Robert G. Ruff
Medical Devices & Rad Health Form 483

FDA 483 Stryker Howmedica Osteonics Corp., Mahwah | 2009

Out-of-stock
Robert G. Ruff
Medical Devices & Rad Health Form 483

FDA 483 Maquet Cardiovascular, LLC, Wayne | 2009

Out-of-stock
Robert G. Ruff
Medical Devices & Rad Health Form 483

FDA 483 Parker Laboratories, Inc., Fairfield | 2009

Out-of-stock
Robert G. Ruff
Medical Devices & Rad Health Form 483