FDA Investigator: Ronald R. Ruff

- Ronald R. Ruff first started conducting FDA inspections in 2000, with the last inspection in 2005. Over that time, Ronald R. Ruff has conducted 79 inspections at 63 companies across 63 sites.

Get Ronald 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 Covance Laboratories, Inc., Madison | 2005

Out-of-stock
Ronald R. Ruff
Human Drug Form 483

FDA 483 Sturm, Christopher D., M.D., Clinical Investigator, Janesville | 2004

Out-of-stock
Ronald R. Ruff
Medical Devices & Rad Health Form 483

FDA 483 Maiman, Dennis J., M.D., Clinical Investigator, Milwaukee | 2004

Out-of-stock
Ronald R. Ruff
Medical Devices & Rad Health Form 483

FDA 483 Murtaugh, Thomas E., M.D., Clinical Investigator, Madison | 2004

Out-of-stock
Ronald R. Ruff
Human Drug Form 483

FDA 483 Bridson, William MD, Clinical Investigator, Madison | 2004

Out-of-stock
Ronald R. Ruff
Human Drug Form 483

FDA 483 Geneva Laboratories, Inc, Elkhorn | 2003

Out-of-stock
Ronald R. Ruff
Medical Devices & Rad Health Form 483