FDA Investigator: Kathy E. Noe
- Kathy E. Noe first started conducting FDA inspections in 2001, with the last inspection in 2003. Over that time, Kathy E. Noe has conducted 6 inspections at 5 companies across 5 sites.
Get Kathy Noe'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 Eli Lilly Italia SPA, Florence | 2002
Out-of-stock
Kathy E. Noe
Human Drug Form 483
FDA 483 Lilly France S.A.S., Fegersheim | 2002
Out-of-stock
Kathy E. Noe
Human Drug Form 483
FDA 483 Vetter Pharma Fertigung GmbH & Co. KG, Ravensburg | 2001
Out-of-stock
Kathy E. Noe
Human Drug Form 483
FDA 483 Sanofi Winthrop Industrie, Maisons-Alfort | 2001
Out-of-stock
Kathy E. Noe
Human Drug Form 483