FDA Investigator: Diana M. Guidry
- Diana M. Guidry first started conducting FDA inspections in 2009, with the last inspection in 2017. Over that time, Diana M. Guidry has conducted 126 inspections at 111 companies across 120 sites.
Get Diana Guidry'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 We Care Designs, Mandeville | June 2014
Available Now - $199
Diana M. Guidry
Medical Devices & Rad Health Form 483
Co-Investigators (24)
- Gabriel E. Muniz, FDA Investigator
- Diana M. Raman, FDA Investigator
- Jason D. Tenney, FDA Investigator
- Audra J. Lenhart, FDA Investigator
- Kimberly C. Delk-Brooks, FDA Investigator
- Justin A. Heffernan, FDA Investigator
- Bonnie E. Pierson, FDA Investigator
- Bonnie E. Conley, FDA Investigator
- Barbara D. Wright, FDA Investigator
- Wanda B. Coats, FDA Investigator
- Daphne A. Videau, FDA Investigator
- Marshall H. Kinsey, FDA Investigator
- Wayne S. Fortenberry, FDA Investigator
- Claire M. Minden, FDA Investigator
- Elizabeth D. Connell, FDA Investigator
- Brian R. Cronenwett, FDA Investigator
- James J. Houlihan, FDA Investigator
- Robert R. Wilson, FDA Investigator
- Kara L. Roden, FDA Investigator
- Weston K. Szymanski, FDA Investigator
- Patrick L. Wisor, FDA Investigator
- Dana D. Carter, FDA Investigator
- Melva J. Palmer, FDA Investigator
- Jessica L. Peterson, FDA Investigator