FDA Investigator Mei Siu
Mei Siu has inspections in 1 countries as of 04 Sep 2015. Mei Siu has collaborated with a combined 308 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
3
Last Inspection Date:
04 Sep 2015
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Arnold C Shih,
Hei Chi Siu,
Jane S Wernberg,
Jasmine N Thompson,
Jeff M Uriarte,
John A Gonzalez,
John A Liu,
Ka L Wong,
Khanh T Van,
M Jasnethoson Thompson,
Mei Chi Siu,
Michael S Araneta,
Michael S Aranota,
Mihaly S Ligmind,
Mihaly S Ligmond,
Sue Lee Chan,
Sumit Sen,
Virgilio F Pacio, CSO,
Yumi J Hiramine
Mei Siu's Documents
Publish Date | Document Type | Title |
---|---|---|
December, 2000 | FDA 483 | Weber Laboratories Inc - Form 483, 2000-12-07 |
December, 2000 | FDA 483 Response | Weber Laboratories Inc - Form 483R, 2001-07-25 |
December, 2000 | EIR | Weber Laboratories Inc - EIR, 2000-12-07 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
![FDA Investigator Profile Icon](https://redica.com/document-store/images/InspectorProfile.png)
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more