FDA Investigator: Mei-Chen Mu

- Mei-Chen Mu first started conducting FDA inspections in 2002, with the last inspection in 2010. Over that time, Mei-Chen Mu has conducted 57 inspections at 51 companies across 52 sites.

Get Mei-Chen Mu'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 Kentec Medical, Inc, Irvine | 2009

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Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 Healthtronics, Inc., Austin | 2009

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Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 Advanced Sterilization Products, Irvine | 2009

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Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 Healthtronics, Inc., Austin | 2009

Out-of-stock
Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 Samsung Medison America Inc, Ridgefield Park | 2008

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Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 American Optisurgical Inc, Lake Forest | 2008

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Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 Merlin Labs, Inc., Carlsbad | 2008

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Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 Cardiomedics Incorporated, Irvine | 2008

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Mei-Chen Mu
Medical Devices & Rad Health Form 483

FDA 483 TMX Engineering & Manufacturing Inc, Santa Ana | 2005

Out-of-stock
Mei-Chen Mu
Medical Devices & Rad Health Form 483