FDA Investigator Cecilia H Kieu
Cecilia H Kieu has inspections in 1 countries as of 01 Nov 2023. Cecilia H Kieu has collaborated with a combined 870 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
11
Last Inspection Date:
01 Nov 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Alanna Lmussawwir Bias,
Alexandra B Pitkin,
Andrea J Schmidt,
Babajide Michael Osunsanmi,
Barbara J White,
Carla J Lundi,
Carr Sharpe,
Carrie A Hughes,
Caryn M Mcnab,
Christopher M Jenner,
Daniel J Lahar,
Deborah A Greco,
Dejon N Harris,
Diane Cvan Leeuwen,
Djamila Harouaka,
Dustin M James,
Edith M Gonzalez,
Isabel Y Espinosa,
James B Arnett,
Jeffrey P Raimondi,
John A Gonzalez,
Jolanna A Norton,
Juanita Banuelos,
Katherine E Jacobitz,
Kelley,
Kham Phommachanh,
Kim Lthomas Cruse,
Langer,
Laurimer Kuilan Torres,
Liming Zhang,
Linda Thai,
Marcus F Yambot,
Michael R Goga,
Minh D Phan,
Nicholas L Hunt,
Patricia F Alberico,
Randall N Johnson,
Roger F Zabinski,
Sangeeta M Khurana, PhD,
Santiago Gallardo Johnson,
Santos E Camara,
Scott N Lim,
Timothy T Kapsala,
Victoria L Palmer,
Virgilio F Pacio, CSO,
Walden H Lee,
Yasamin Ameri,
Zachary A Bogorad,
Zachary L Stamm
Cecilia H Kieu's Documents
Publish Date | Document Type | Title |
---|---|---|
September, 2023 | FDA 483 | PETNET SOLUTIONS, INC. - Form 483, 2023-09-08 |
March, 2023 | EIR | Bachem Americas, Inc. - EIR, 2023-03-27 |
August, 2021 | FDA 483 | Blaine Labs Inc. - Form 483, 2021-08-24 |
June, 2023 | FDA 483 | Calvin Scott & Co., Inc. - Form 483, 2023-06-19 |
March, 2023 | FDA 483 | Bachem Americas, Inc. - Form 483, 2023-03-27 |
December, 2022 | FDA 483 | 220 Laboratories LLC. - Form 483, 2022-12-22 |
September, 2022 | FDA 483 | Valor Compounding Pharmacy, Inc DBA Valor Compounding Pharmacy - Form 483, 2022-09-15 |
March, 2022 | FDA 483 | Airgas Usa, LLC - Form 483, 2022-03-11 |
September, 2023 | FDA 483 | RLC Labs Inc. - Form 483, 2023-09-15 |
November, 2023 | FDA 483 | RLC Labs Inc. - Form 483, 2023-11-02 |
September, 2023 | FDA 483 | RLC Labs Inc. - Form 483, 2023-09-15 |
December, 2023 | FDA 483 | B. Braun Medical Inc. - Form 483, 2023-12-15 |
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