FDA Investigator Viviana R Ramirez

Viviana R Ramirez has conducted inspections on 8 sites in 5 countries as of 28 May 2024. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
8
Last Inspection Date:
28 May 2024
Investigator Role:
FDA Investigator
Redica ID:
100010609
Countries of Inspections:
France, United States of America, Italy, Spain, Denmark
FDA Investigators that have inspected at least one site in common with Viviana R Ramirez:
Andrew Byrnes, PhD, Anissa M Cheung, Anna R Kwilas, Anthony F Lorenzo, Arsen Karapetyan, Bharat Khurana, Bo Liang, PhD, Burnell M Henry, Carla A Norris, Caryn M Mcnab, Christelle Mbondji Wonje, Christopher T Peters, Claire M Minden, Demitria J Xiradakis, Denise M Digiulio, Donald C Obenhuber, PhD, Dorothy P Kramer, Dr. Zhihao Qiu (Peter), PhD, Elvira R Argus, Emmanuel Adu Gyamfi, PhD, Erin C Hill, Gene D Arcy, Grace I Cortesini, Graeme E Price, Graeme Price, Hector A Carrero, Jacob L Bitterman, Jared D Greenleaf, Jennifer Lalama, Kathleen M Jordan, Kevin J Matthews, Lauren N Barber, Lawrence J Stringer, LCDR Chad N Thompson, LCDR Debra Emerson, Lewis K Antwi, Lily Y Koo, Lydia I Rosas Marty, Marie F Morin, Megan A Haggerty, Michael Shanks, MS, Monica Commerford, PhD, Nirjal Bhattarai, Pankaj H Amin, Patricia F Hughes, PhD, Paul L Bellamy, Priscilla M Pastrana, Randa Melhem, PhD, Raymond T Oji, Robert J Martin, Sean R Marcsisin, Stephanie Mangigian, MS/OSH, RN, Stephen D Brown, Sukyoung Sohn, Susan M Jackson, Temar Q Williams, Thai D Truong, Thuy T Nguyen, LCDR, Tiffany M Lucas, Unnee Ranjan, Viviana Matta, Wanda E Pagan, PhD, Zhongren Wu

Viviana R Ramirez's Documents

Publish Date Document Type Title
March, 2023 FDA 483 Catalent Maryland, Inc. - Form 483, 2023-03-10
May, 2023 FDA 483 Bristol-Myers Squibb Company - Form 483, 2023-05-05

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