Kelly R. Lewis
FDA Investigator
- Kelly R. Lewis first started conducting FDA inspections in 2012, with the last inspection in 2013. Over that time, Kelly R. Lewis has conducted 2 inspections at 2 companies across 2 sites.
Get Kelly Lewis'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 Pfizer Ireland Pharmaceuticals, Dublin 22 | 2013
Out of stock
FDA 483 Protein Sciences Corporation, Meriden | 2012
Out of stock