Kathy Kuo

FDA Investigator

- Kathy Kuo first started conducting FDA inspections in 2016, with the last inspection in 2017. Over that time, Kathy Kuo has conducted 3 inspections at 3 companies across 3 sites.

Get Kathy Kuo'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 PolyPeptide Laboratories, Inc., Torrance | 2017

Out of stock

FDA 483 Nitto Avecia Pharma Services, Inc, Irvine | 2017

Out of stock

FDA 483 Exova Inc., Santa Fe Springs | 2016

Out of stock