FDA Investigator: Gary D. Urbiel Goldner

- Gary D. Urbiel Goldner first started conducting FDA inspections in 2008, with the last inspection in 2012. Over that time, Gary D. Urbiel Goldner has conducted 18 inspections at 15 companies across 15 sites.

Get Gary Urbiel Goldner'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 Zimmer, Warsaw | July 2011

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Gary D. Urbiel Goldner
Medical Devices & Rad Health Form 483

FDA 483 Zimmer, Inc., Warsaw | 2012

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Gary D. Urbiel Goldner
Medical Devices & Rad Health Form 483

FDA 483 Xoran Technologies, Inc., Ann Arbor | 2011

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Gary D. Urbiel Goldner
Medical Devices & Rad Health Form 483

FDA 483 Xoran Technologies, Inc., Ann Arbor | 2010

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Gary D. Urbiel Goldner
Medical Devices & Rad Health Form 483

FDA 483 Rocky Peanut Company, Inc., Ferndale | 2010

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Gary D. Urbiel Goldner
Foods & Cosmetic Form 483

FDA 483 Rocky Peanut Company, Inc., Ferndale | 2010

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Gary D. Urbiel Goldner
Foods & Cosmetic Form 483

FDA 483 Terumo Cardiovascular Systems Corporation, Ann Arbor | 2010

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Gary D. Urbiel Goldner
Medical Devices & Rad Health Form 483

FDA 483 Cybernet Medical Corp., Ann Arbor | 2009

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Gary D. Urbiel Goldner
Medical Devices & Rad Health Form 483

FDA 483 Pointe Scientific, Inc., Canton | 2009

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Gary D. Urbiel Goldner
Medical Devices & Rad Health Form 483

FDA 483 Henry Ford Reproductive Medicine, Troy | 2008

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Gary D. Urbiel Goldner
Biologic Form 483