FDA Investigator Deborah Schmiel, PhD

Deborah Schmiel, PhD has conducted inspections on 4 sites in 3 countries as of 07 Oct 2019. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
4
Last Inspection Date:
07 Oct 2019
Investigator Role:
FDA Investigation Participant
Redica ID:
100003981
Countries of Inspections:
Korea (Republic of), Austria, Denmark
FDA Investigators that have inspected at least one site in common with Deborah Schmiel, PhD:
Alicia M Mozzachio, Anjali Shukla, PhD, Bo Chi, PhD, Brandon C Heitmeier, Brian M Janelsins, PhD, Carla J Lundi, Christopher Downey, PhD, Dennis Cantellops Paite, Diane L Raccasi, Dogbeda F Mackenzie, Dr. Ralph M Bernstein, PhD, Ephrem Hunde, PhD, Hyung Yul Lee, Jacek Cieslak, PhD, Jeffrey P Raimondi, Jennifer M Gogley, Laura Fontan, MS, Laurel A Beer, Linda F Murphy, Lucila B Nwatu, Madushini Dharmasena, PhD, Maria Gutierrez Lugo, PhD, Maria Joselopez Barragan, PhD, Marion Michaelis, Marjorie A Shapiro, PhD, Maryam Tabatabaie, Matthew B Casale, Michael Shanks, MS, Monica Markovski, PhD, Mra B Kamberem, Mra V Millarw, Patrick J Lynch, Paul L Bellamy, Peter Adams, PhD, Phillip Angart, PhD, Prabhu P Raju, Rashmi Rawat, PhD, Rebecca Rodriguez, Reyes Candau Chacon, PhD, Riley C Myers, PhD, Sarah Arden, Sarah Kennett, PhD, Scott R Nichols, PhD, Steven Fong, MS, PhD, Thuy T Nguyen, LCDR, Virginia Carroll, PhD, Wayne E Seifert, William Hallett, PhD, Xianghong Jing (Emily), PhD, Xiaoping Guan, Yehualashet A Gessesse, Yun Wu, PhD, Zhong Li, PhD

Deborah Schmiel, PhD's Documents

Publish Date Document Type Title
June, 2016 FDA 483 Samsung Biologics Co., Ltd. - Form 483, 2016-06-22
October, 2019 FDA 483 FUJIFILM Diosynth Biotechnologies Denmark ApS - Form 483, 2019-10-11
February, 2018 FDA 483 Sandoz GmbH - Form 483, 2018-02-20
June, 2018 FDA 483 Samsung Biologics Co., Ltd. - Form 483, 2018-06-26
February, 2024 FDA 483 BSP Pharmaceuticals SpA - Form 483, 2024-02-29

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