FDA Investigator Diane P Goyette

Diane P Goyette has conducted inspections on 3 sites in 1 countries as of 17 Apr 2017. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
3
Last Inspection Date:
17 Apr 2017
Investigator Role:
FDA Investigator
Redica ID:
100003825
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Diane P Goyette:
Abdollah Koolivand, Bonita S Chester, Brandon C Heitmeier, Clifton L Randell, Constance Y Fears, Demario L Walls, Desiree D Clark, Edith M Gonzalez, Frank Wackes, George J Flynn, Jamie L Port, Jared P Stevens, Jennifer Lalama, Jessica L Pressley, June P Page, Kemejumaka N Opara, Lareese K Thomas, Larry K Hampton, Margaret M Annes, Marvin D Jones, Mary Jeanet Mcgarry, Melanie M Walker, Narong Chamkasem, PhD, Nicole A Lloyd, Noreen Muñiz, Postelle Birch Smith, Rachael L Cook, Regan T Harp, Saundrea A Munroe, Sayeeda Hdabe, Seneca D Toms, Sharna D Pratt, Song Y Lavalais, Sonya M Edmonds, Steven D Dittert, Vincent Thomas, Wayne S Fortenberry, Zachary L Miller, Zada L Giles

Diane P Goyette's Documents

Publish Date Document Type Title
February, 2017 FDA 483 Response Delta Pharma, Inc. - Form 483R, 2017-03-15
April, 2017 EIR Nephron Sterile Compounding Center, LLC - EIR, 2017-04-21
April, 2017 FDA 483 Nephron Sterile Compounding Center, LLC - Form 483, 2017-04-21
February, 2017 FDA 483 Delta Pharma, Inc. - Form 483, 2017-02-23

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