FDA Investigator: Heika R. Tait

- Heika R. Tait first started conducting FDA inspections in 2002, with the last inspection in 2014. Over that time, Heika R. Tait has conducted 174 inspections at 147 companies across 150 sites.

Get Heika Tait'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 Hikma Farmaceutica, (Portugal) S.A., Terrugem Snt | 2014

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Heika R. Tait
Human Drug Form 483

FDA 483 Pharmachemie B.V., Haarlem | 2013

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Heika R. Tait
Human Drug Form 483

FDA 483 Pharmachemie B.V., Haarlem | 2013

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Heika R. Tait
Human Drug Form 483

FDA 483 Merck Sante, Semoy | 2013

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Heika R. Tait
Human Drug Form 483

FDA 483 Merck Sante s.a.s, Semoy Cedex | 2013

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Heika R. Tait
Human Drug Form 483

FDA 483 Genzyme A Sanofi Company, Lynnwood | 2013

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Heika R. Tait
Human Drug Form 483

FDA 483 Pascal Co Inc, Bellevue | 2013

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Heika R. Tait
Human Drug Form 483

FDA 483 Dipharma Francis S.r.l., Caronno Pertusella | 2012

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Heika R. Tait
Human Drug Form 483

FDA 483 Merazon Health Products Inc, Seattle | 2012

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Heika R. Tait
Human Drug Form 483

FDA 483 Univar USA Inc., Kent | 2011

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Heika R. Tait
Human Drug Form 483

FDA 483 Comprehensive Clinical Development Northwest, Inc, Tacoma | 2011

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Heika R. Tait
Human Drug Form 483

Co-Investigators (50)