FDA Investigator: Rapti D. Madurawe
- Rapti D. Madurawe first started conducting FDA inspections in 2017, with the last inspection in 2018. Over that time, Rapti D. Madurawe has conducted 2 inspections at 2 companies across 2 sites.
Get Rapti Madurawe'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 Lilly del Caribe, . (PR01, Carolina | July 2017
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Rapti D. Madurawe
Human Drug Form 483
FDA 483 Pfizer Inc, Groton | 2018
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Rapti D. Madurawe
Human Drug Form 483