FDA Investigator: Karen A. Coleman

- Karen A. Coleman first started conducting FDA inspections in 2000, with the last inspection in 2007. Over that time, Karen A. Coleman has conducted 54 inspections at 42 companies across 43 sites.

Get Karen Coleman'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 Vapotherm, Inc., Stevensville | 2007

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 Ion Beam Applications S.A., Louvain La Neuve | 2006

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 Hitachi Medical Systems, Kashiwa City | 2006

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 Pentax Corporation, Tokyo | 2006

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 B.F. Wehmer Company, Inc., Lombard | 2005

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 CryoLife, Inc., Kennesaw | 2005

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Karen A. Coleman
Biologic Form 483

FDA 483 bioMerieux, Inc., Durham | 2005

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 Best Vascular, Inc, Norcross | 2004

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 Wako Pure Chemical Industries, Ltd. (Mie Plant), Mie-Gun, Mie Pref. | 2004

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 ITO Co., Ltd. (Tsukuba Factory), Inashiki-gun, Ibaraki-ken | 2004

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 bioMerieux, Inc., Durham | 2004

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Karen A. Coleman
Medical Devices & Rad Health Form 483

FDA 483 CryoLife, Inc., Kennesaw | 2004

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Karen A. Coleman
Biologic Form 483