FDA Investigator Kimberly L Schultz
Kimberly L Schultz has conducted inspections on 4 sites in 1 countries as of 28 Nov 2023. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
4
Last Inspection Date:
28 Nov 2023
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Kimberly L Schultz:
Addam S Reynolds,
Alberto A Viciedo,
Anna R Kwilas,
Ashley J Burns,
Byungja E Marciante,
Christopher R Czajka,
Colleen F Hoyt,
David E Bailey,
Dawn L Wydner,
Denis Gavin, PhD,
Dorothy J Denes,
Eileen A Liu,
Emily A Walters,
Erin D Mccaffery,
Haley H Seymour,
Helen B Ricalde,
Jacqueline Mdiaz Albertini,
Joan Johnson,
Jose M Cayuela,
Justine Tomasso,
Latorie S Jones,
Linda Thai,
Margaret M Sands,
Melissa T Roy,
Michael S Araneta,
Michael Serrano,
Michelle A Marsh,
Nicholas A Violand,
Nimmy Mathews,
Nina Yang,
Nirjal Bhattarai,
Peter R Lenahan,
Prabhu P Raju,
Rabia Ballica, PhD,
Randa Melhem, PhD,
Ruth A Williams,
Susan M Jackson,
Thai D Truong,
Travis S Bradley,
Tyanna N Hadley,
Unnee Ranjan,
Xiaobin Lu (Victor), PhD
Kimberly L Schultz's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| August, 2019 | EIR | Novartis Pharmaceuticals Corporation - EIR, 2019-08-21 |
| February, 2021 | EIR | CELGENE CORPORATION - EIR, 2021-03-10 |
| August, 2019 | FDA 483 | Novartis Pharmaceuticals Corporation - Form 483, 2019-08-21 |
| August, 2019 | FDA 483 Response | Novartis Pharmaceuticals Corporation - Form 483R, 2019-09-12 |
| October, 2020 | FDA 483 Response | Juno Therapeutics, Inc. - Form 483R, 2020-11-05 |
| October, 2020 | EIR | Juno Therapeutics, Inc. - EIR, 2020-10-16 |
| December, 2023 | FDA 483 | Carsgen Therapeutics Corporation - Form 483, 2023-12-06 |
| February, 2021 | FDA 483 Response | CELGENE CORPORATION - Form 483R, 2021-03-11 |
| October, 2020 | FDA 483 | Juno Therapeutics, Inc. - Form 483, 2020-10-16 |
| February, 2021 | FDA 483 | CELGENE CORPORATION - Form 483, 2021-02-19 |
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