FDA Investigator: Lori P. Peters
- Lori P. Peters first started conducting FDA inspections in 2009, with the last inspection in 2022. Over that time, Lori P. Peters has conducted 8 inspections at 8 companies across 7 sites.
Get Lori Peters's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
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FDA 483 Imugen, Inc, Norwood | 2017
Out-of-stock
Lori P. Peters
Medical Devices & Rad Health Form 483
FDA 483 Protein Sciences, Pearl River | 2015
Out-of-stock
Lori P. Peters
Biologic Form 483
FDA 483 Avioq, Inc., Research Triangle Par | 2012
Out-of-stock
Lori P. Peters
Biologic Form 483
FDA 483 Kedrion S.p.A., Bolognana | 2011
Out-of-stock
Lori P. Peters
Biologic Form 483
FDA 483 Maxim Biomedical Incorporated, Rockville | 2010
Out-of-stock
Lori P. Peters
Biologic Form 483
FDA 483 Instituto Bioclon, S.A. de C.V., Mexico | 2009
Out-of-stock
Lori P. Peters
Biologic Form 483
Co-Investigators (9)
- Kathleen R. Jones, FDA Investigator
- Miriam M. Ngundi, FDA Investigator
- Justine M. Corson, FDA Consumer Safety Officer
- Christine Harman, FDA Investigator
- Sean R. Byrd, FDA Investigator
- Nicole K. Trudel, FDA Investigator
- Qiao Y. Bobo, FDA Investigator
- Nancy T. Waites, FDA Investigator
- Martha T. Olone, FDA Investigator