FDA Investigator Lillian C Hsu
Lillian C Hsu has conducted inspections on 10 sites in 1 countries as of 28 May 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
10
Last Inspection Date:
28 May 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Lillian C Hsu:
Alexandra B Pitkin,
Alexis S Roberts,
Amanda B Athey,
Amanda M Osteen,
Amos C Epps,
Andre L Duhon,
April R Bowen,
Barbara S Manson,
Brian R Yaun,
Carrie L Doupnik,
Catherine M Vanderhoef,
Christina H Owens,
Christopher M Henderson,
Combs,
Conrad M Guardia,
Daphne A Videau,
Darrah,
David J Leray,
Debra D Devlieger,
Diana K Krepel,
Dianne H Milazzo,
Dwayne A Miller,
Eric C Fox,
Eric C Nielsen,
Erik T Nagaoka,
Esaw,
Francis A Guidry,
Frederick J Tillman,
Gifford Whitehurst, Jr,
Gina M Scholze,
Heath A Gerber,
Herbert M Corbello,
Hokenson,
Howard A Burmester,
Jacob A Clark,
Jamie R Thompson,
Jessica D Weber,
Jessica E Hensley,
Jessica L Barr,
Johnson,
Jose R Hernandez,
Joseph F Owens,
Karen A Spencer,
Katherine A Clarke Girolamo,
Katherine M Taylor,
Kathryn A Cutajar,
Keri U Walker,
LCDR Matthew R Mcnew, MPH, REHS/RS,
LCDR Wilfred A Darang,
Lillian Hsu,
Linda S Jozefiak,
Linhart,
Mahaffey,
Marcus A Ray,
Marla A Cassidy,
Marlon K Turner,
Matthew L Doyle,
Matthew R Noonan,
Melanie C Voges,
N'jere English,
Neali H Lucas,
Nicholas J Dubrovin,
Owens,
Priya J Rathnam,
Rebecca L Mullikin,
Renisha M Shaw,
Robert Q Green,
Sandra I Gaul,
Scott T Ballard,
Sean R Moynihan, MPH,
Shafiq S Ahadi,
Sherry R Dunn,
Sierra M Shockley,
Stephen C Eason,
Steven W Brown,
Tamara N Champion,
Thomas R Withers,
Thuy T Nguyen, LCDR,
Tiki J Dixon,
Walsworth,
William A Warnick,
William E Keer
Lillian C Hsu's Documents
Publish Date | Document Type | Title |
---|---|---|
June, 2017 | FDA 483 | Gilster Mary Lee Corp-Cereal Plant - Form 483, 2017-06-22 |
June, 2017 | EIR | Gilster Mary Lee Corp-Cereal Plant - EIR, 2017-06-22 |
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](/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