FDA Investigator: Lisa C. Lewis
- Lisa C. Lewis first started conducting FDA inspections in 2002, with the last inspection in 2003. Over that time, Lisa C. Lewis has conducted 15 inspections at 13 companies across 12 sites.
Get Lisa Lewis's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
Upon purchase, you will receive an email with a link to immediately download the documents.
FDA 483 Xttrium Laboratories, Inc., Chicago | 2003
Out-of-stock
Lisa C. Lewis
Human Drug Form 483
FDA 483 Jin Han International Inc., Chicago | 2003
Out-of-stock
Lisa C. Lewis
Foods & Cosmetic Form 483
FDA 483 Akorn, Inc., Lake Forest | 2003
Out-of-stock
Lisa C. Lewis
Human Drug Form 483
FDA 483 Ray, Paul Schumann, DO, Chicago | 2002
Out-of-stock
Lisa C. Lewis
Human Drug Form 483
FDA 483 Airgas North Central, Inc., West Chicago | 2002
Out-of-stock
Lisa C. Lewis
Human Drug Form 483