FDA Investigator: Devaughn Edwards
- Devaughn Edwards first started conducting FDA inspections in 2000, with the last inspection in 2006. Over that time, Devaughn Edwards has conducted 134 inspections at 91 companies across 98 sites.
Get Devaughn Edwards'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 Catalent Germany Schomdorf GmbH, Schorndorf | 2005
Out-of-stock
Devaughn Edwards
Human Drug Form 483
FDA 483 Hospira, Inc., Rocky Mount | 2005
Out-of-stock
Devaughn Edwards
Human Drug Form 483
FDA 483 Banner Pharmacaps Inc., High Point | 2005
Out-of-stock
Devaughn Edwards
Human Drug Form 483
FDA 483 Banner Pharmacaps Inc., Greensboro | 2005
Out-of-stock
Devaughn Edwards
Human Drug Form 483
Co-Investigators (12)
- Parul M. Patel, FDA Investigator
- Michelle D. Haamid, FDA Investigator
- Edecia A. Richards, FDA Investigator
- Thomas R. Berry, FDA Investigator
- Jawaid Hamid, FDA Investigator
- Robert C. Coleman, FDA Investigator
- Philip F. Istafanos, FDA Investigator
- Amy H. Ruble, FDA Investigator
- Cheryl D. Barton, FDA Investigator
- Eric S. Weilage, FDA Investigator
- Samuel T. Walker, FDA Investigator
- Kathleen D. Culver, FDA Investigator