FDA Investigator: Unnee Ranjan

- Unnee Ranjan first started conducting FDA inspections in 2014, with the last inspection in 2024. Over that time, Unnee Ranjan has conducted 93 inspections at 86 companies across 90 sites.

Get Unnee Ranjan'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 Genzyme Corporation, Ridgefield | 2024

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Unnee Ranjan
Biologics Form 483

FDA 483 SmithKline Beecham Pharma GmbH & co. KG (dba GlaxoSmithKline Biologicals), Dresden | 2024

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Unnee Ranjan
Biologics Form 483

FDA 483 GSK Vaccines GmbH, Marburg | 2024

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Unnee Ranjan
Biologics Form 483

FDA 483 Novartis Gene Therapies, Inc., Durham | 2024

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Unnee Ranjan
Biologics Form 483

FDA 483 Sanofi Winthrop Industrie, Lyon | 2023

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Unnee Ranjan
Biologics Form 483

FDA 483 Bavarian Nordic A/S, Kvistgard | 2023

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Unnee Ranjan
Biologics Form 483

FDA 483 Novo Nordisk A/S, Kalundborg | 2023

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Unnee Ranjan
Biologics Form 483

FDA 483 Sanofi Winthrop Industrie, Le Trait | 2023

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Unnee Ranjan
Biologics Form 483

FDA 483 Recipharm AB, Oeiras | 2023

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Unnee Ranjan
Biologics Form 483

FDA 483 GlaxoSmithKline Biologicals, Dresden | 2022

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Unnee Ranjan
Biologic Form 483

FDA 483 Uniqure Inc, Lexington | 2022

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Unnee Ranjan
Biologics Form 483

FDA 483 AstraZeneca Pharmaceuticals, LP, Philadelphia | 2022

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Unnee Ranjan
Biologic Form 483

FDA 483 Aptar Radolfzell Gmbh, Eigeltingen | 2022

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Unnee Ranjan
Human Drug Form 483

Co-Investigators (54)