FDA Investigator: Matthew R. Sleeter

- Matthew R. Sleeter first started conducting FDA inspections in 2004, with the last inspection in 2013. Over that time, Matthew R. Sleeter has conducted 28 inspections at 22 companies across 24 sites.

Get Matthew Sleeter'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 Nostrum Laboratories, Inc., Kansas City | 2010

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Matthew R. Sleeter
Human Drug Form 483

FDA 483 VVF Kansas Services LLC, Kansas City | 2010

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Matthew R. Sleeter
Human Drug Form 483

FDA 483 Nostrum Laboratories, Inc., Kansas City | 2009

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Matthew R. Sleeter
Human Drug Form 483

FDA 483 Custom Industrial Analysis Labs Inc, Saint Joseph | 2009

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Matthew R. Sleeter
Animal Drugs & Feed Form 483

FDA 483 Community Blood Center Of Gtr KC, Kansas City | 2009

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Matthew R. Sleeter
Biologic Form 483

FDA 483 Nostrum Laboratories, Inc., Kansas City | 2008

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Matthew R. Sleeter
Human Drug Form 483

FDA 483 PolyPeptide Laboratories A/S, Hillerod | 2008

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Matthew R. Sleeter
Human Drug Form 483

FDA 483 Scanpharm, Birkerod | 2008

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Matthew R. Sleeter
Human Drug Form 483

FDA 483 Fresenius Kabi Austria Gmbh, Linz | 2008

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Matthew R. Sleeter
Human Drug Form 483