FDA Investigator: Mary-Ann Ruff
- Mary-Ann Ruff first started conducting FDA inspections in 2000, with the last inspection in 2005. Over that time, Mary-Ann Ruff has conducted 110 inspections at 51 companies across 65 sites.
Get Mary-Ann Ruff'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 BloodCenter of Wisconsin, Inc, Milwaukee | 2004
Out-of-stock
Mary-Ann Ruff
Biologic Form 483
FDA 483 Innovative Blood Resources, Saint Paul | 2003
Out-of-stock
Mary-Ann Ruff
Biologic Form 483
FDA 483 Community Health Network - Berlin Memorial Hospital, Berlin | 2003
Out-of-stock
Mary-Ann Ruff
Biologic Form 483
Co-Investigators (15)
- Jesse P. Romenesko, FDA Investigator
- Denise L. Burosh, FDA Investigator
- Darlene L. Krieger, FDA Investigator
- Kellie L. Westerbuhr, FDA Investigator
- Charles Cote, FDA Investigator
- Scott B. Laufenberg, FDA Investigator
- Jon C. Polzine, FDA Investigator
- Jeffery A. Hangartner, FDA Investigator
- Jeffry A. Bernhardt, FDA Investigator
- Cntrctmntr Como, FDA Investigator
- Melissa D. Kalik, FDA Investigator
- Demetria L. Lueneburg, FDA Investigator
- Elizabeth E. Hart, FDA Investigator
- John P. Hermann, FDA Investigator
- Howard A. Burmester, FDA Investigator