FDA Investigator: Kristen E. Rescigno

- Kristen E. Rescigno first started conducting FDA inspections in 2009, with the last inspection in 2014. Over that time, Kristen E. Rescigno has conducted 52 inspections at 43 companies across 42 sites.

Get Kristen Rescigno'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 Burpee Materials Technology, LLC, Eatontown | 2014

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Biological Controls, Eatontown | 2014

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Convatec, Greensboro | 2014

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Maquet Cardiovascular, LLC, Wayne | 2013

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Maquet Medical Systems USA, Wayne | 2013

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Paragon Packaging, Inc., Carteret | 2013

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Kristen E. Rescigno
Human Drug Form 483

FDA 483 McNeil PPC Inc., Skillman | 2013

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 ConvaTec, Inc, Skillman | 2013

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Replication Medical, Inc., Cranbury | 2012

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 CNSystems Medizintechnik AG, Graz | 2012

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Renishaw plc, Wotton-under-edge | 2012

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483

FDA 483 Philips Electronics Ltd., Toronto | 2012

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Kristen E. Rescigno
Medical Devices & Rad Health Form 483