FDA Investigator: Sue Lee Chan

- Sue Lee Chan first started conducting FDA inspections in 2000, with the last inspection in 2004. Over that time, Sue Lee Chan has conducted 13 inspections at 13 companies across 13 sites.

Get Sue Lee Chan'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 Amphastar Pharmaceuticals, Inc., Rancho Cucamonga | 2004

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Nippon Aerosil Co., Ltd., Yokkaichi Mie | 2004

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Mitsubishi Pharma, Iwaki-City | 2004

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Exova Inc., Santa Fe Springs | 2002

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Abraxis Bioscience Llc, Phoenix | 2002

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Bio-science Research Institute, Inc, Chino | 2002

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Watson Laboratories, Inc., Corona | 2001

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Weber Laboratories Inc, Irvine | 2000

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Apotex Pharmachem Inc., Brantford | 2000

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Apotex Inc., Toronto | 2000

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Ajinomoto Co., Inc., Yokkaichi | 2000

Out-of-stock
Sue Lee Chan
Human Drug Form 483

FDA 483 Tanaka Kikinzoku Kogyo Co., Ltd., Kanagawa | 2000

Out-of-stock
Sue Lee Chan
Human Drug Form 483