FDA Investigator: Barbara J. Holladay
- Barbara J. Holladay first started conducting FDA inspections in 2000, with the last inspection in 2004. Over that time, Barbara J. Holladay has conducted 116 inspections at 93 companies across 94 sites.
Get Barbara Holladay'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 Covance Laboratories, Inc., Chantilly | 2004
Out-of-stock
Barbara J. Holladay
Human Drug Form 483
FDA 483 Robert B Innis MD, Bethesda | 2004
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Barbara J. Holladay
Human Drug Form 483
FDA 483 U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick | 2003
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Barbara J. Holladay
Biologic Form 483
FDA 483 Douglas R Rosing MD, Bethesda | 2003
Out-of-stock
Barbara J. Holladay
Human Drug Form 483
FDA 483 Armed Forces Institute of Pathology, Washington | 2003
Out-of-stock
Barbara J. Holladay
Medical Devices & Rad Health Form 483
FDA 483 Bruce Rind MD, Washington | 2003
Out-of-stock
Barbara J. Holladay
Medical Devices & Rad Health Form 483
FDA 483 Malcolm Grow Medical Center, Andrews AFB | 2003
Out-of-stock
Barbara J. Holladay
Human Drug Form 483
Co-Investigators (12)
- John M. Gusto, FDA Investigator
- Lorraine L. Chavis, FDA Investigator
- Charles M. Kerns, FDA Investigator
- Kenneth Nieves, FDA Investigator
- Ronald T. Nowalk, FDA Investigator
- Regina G. Melton, FDA Investigator
- Wayne L. Jefferson, FDA Investigator
- Melanie M. Mayor, FDA Investigator
- Christine M. Smith, FDA Investigator
- Linda J. Eason, FDA Investigator
- Barbara A. Burke, FDA Investigator
- Bruce C. Kovak, FDA Investigator