FDA Investigator: Diane P. Goyette
- Diane P. Goyette first started conducting FDA inspections in 2014, with the last inspection in 2017. Over that time, Diane P. Goyette has conducted 3 inspections at 3 companies across 3 sites.
Get Diane Goyette'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 Nephron Pharmaceuticals, West Columbia | April 2017
Available Now - $199
Diane P. Goyette
Human Drug Form 483
