FDA Documents of NerPharMa S.r.l.
NerPharMa S.r.l. is an organization that has been audited by the FDA 9 times between 2008 and 2024 across all 3 sites.
Documents
FDA 483 NerPharMa S.r.l., Nerviano | 2024
Out-of-stock
Issued on: Jun 19, 2024
Human Drugs Form 483
FDA 483 NerPharMa S.r.l., Nerviano | 2023
Out-of-stock
Issued on: Feb 20, 2023
Human Drugs Form 483
FDA 483 NerPharMa S.r.l., Nerviano | 2017
Out-of-stock
Issued on: Jun 1, 2017
Human Drug Form 483
FDA 483 NerPharMa S.r.l., Nerviano | 2015
Out-of-stock
Issued on: Mar 5, 2015
Human Drug Form 483
FDA 483 NerPharMa S.r.l., Nerviano Milano | 2009
Out-of-stock
Issued on: Oct 30, 2009
Human Drug Form 483
FDA 483 NerPharMa S.r.l., Nerviano Milano | 2008
Out-of-stock
Issued on: Sep 26, 2008
Human Drug Form 483
FDA Investigators(17)
- Jeffrey P. Raimondi, FDA Investigator
- Ruo H. Xu, FDA Investigator
- Daniel L. Obrzut, FDA Investigator
- Cynthia Jim, FDA Investigator
- Susan T. Hadman, FDA Investigator
- Kham Phommachanh, FDA Investigator
- Kejun Cheng, FDA Investigator
- Lucas B. Leake, FDA Investigator
- Junho Pak, FDA Investigator
- Patric C. Klotzbuecher, FDA Investigator
- Brittany D. Terhar, FDA Investigator
- Deborah A. Greco, FDA Investigator
- Carla A. Norris, FDA Investigator
- Susan M. Jackson, FDA Investigator
- Simone E. Pitts, FDA Investigator
- Kristy A. Zielny, FDA Investigator
- Barbara D. Paul, FDA Investigator