FDA Investigator: Robert Sharpnack
- Robert Sharpnack first started conducting FDA inspections in 2000, with the last inspection in 2003. Over that time, Robert Sharpnack has conducted 16 inspections at 16 companies across 16 sites.
Get Robert Sharpnack'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 Pliva, Inc., East Hanover | 2003
Out-of-stock
Robert Sharpnack
Human Drug Form 483
FDA 483 Meridian Bioscience Inc, Cincinnati | 2001
Out-of-stock
Robert Sharpnack
Medical Devices & Rad Health Form 483
FDA 483 Watson Laboratories, Inc., Hialeah | 2000
Out-of-stock
Robert Sharpnack
Human Drug Form 483
Co-Investigators (16)
- Paul L. Bellamy, FDA Investigator
- Ernest Bizjak, FDA Investigator
- Brenda S. Zimmer, FDA Investigator
- Ivis L. Negron Torres, FDA Investigator
- Jose E. Melendez, FDA Investigator
- Margarita Santiago, FDA Investigator
- Negron Torres, Ivis L, FDA Investigator
- Michael J. Kuchta, FDA Investigator
- Frederick L. Fricke, FDA Investigator
- Karen A. Wolnik, FDA Investigator
- Gina M. Brackett, FDA Investigator
- Christopher A. Demitrius, FDA Investigator
- Merril E. Racke, FDA Investigator
- Roy R. Rinc, FDA Investigator
- Joe X. Phillips, FDA Investigator
- Marie T. Falcone, FDA Investigator