FDA Investigator: Karen K. Takahashi

- Karen K. Takahashi first started conducting FDA inspections in 2000, with the last inspection in 2011. Over that time, Karen K. Takahashi has conducted 28 inspections at 27 companies across 27 sites.

Get Karen Takahashi'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 Laboratorios Belmac S.A., Zaragoza | 2006

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Eurofins Dr. Specht Laboratorien, GmbH, Hamburg | 2006

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Karen K. Takahashi
Human Drug Form 483

FDA 483 C.P.M. Contract Pharma GmbH & Co. KG, Feldkirchen-Westerham | 2006

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Hovione PharmaScience Limited, Taipa | 2004

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Formosa Laboratories, Inc., Taoyuan | 2004

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Katayama Seiyakusyo Co., Ltd., Toyama Plant, Nei-gun | 2004

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Steins Laboratorium A/S, Holstebro | 2004

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Danisco A/S, DK-7200 Grindsted | 2004

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Karen K. Takahashi
Human Drug Form 483

FDA 483 FDC, Ltd., Roha, Raigad District | 2003

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Ranbaxy Laboratories Limited (Toansa), Punjab | 2003

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Kunshan Chemicals & Pharmaceutical Factory, Jiangsu | 2002

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Karen K. Takahashi
Human Drug Form 483

FDA 483 Huzhou Zhanwang Pharmaceutical Co., Ltd., Huzhou | 2002

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Karen K. Takahashi
Human Drug Form 483