FDA Investigator Anna R Kwilas
Anna R Kwilas has conducted inspections on 5 sites in 1 countries as of 01 Apr 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
5
Last Inspection Date:
01 Apr 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 Anna R Kwilas:
Addam S Reynolds,
Alberto A Viciedo,
Bo Liang, PhD,
Byungja E Marciante,
Carl A Perez,
Christian D Lynch (CDL),
Dawn L Wydner,
Dorothy J Denes,
Elvira R Argus,
Emily A Walters,
Erin D Mccaffery,
Haley H Seymour,
Helen B Ricalde,
Jakob Reiser, PhD,
Jianyang Wang,
Jie He,
Jose M Cayuela,
Justine Tomasso,
Kimberly L Schultz,
Laura K Demaster,
Lauren M Lilly, PhD,
Linda Thai,
Margaret M Sands,
Melissa T Roy,
Michael Serrano,
Michelle A Marsh,
Nicholas A Violand,
Nimmy Mathews,
Nina Yang,
Nirjal Bhattarai,
Pankaj K Mandal,
Peter R Lenahan,
Phillip C Thai,
Priscilla M Pastrana,
Rabia Ballica, PhD,
Ruth A Williams,
Scott T Ballard,
Sharmila Shrestha,
Stephanie Mangigian, MS/OSH, RN,
Steven E Bowen, PhD,
Tyanna N Hadley,
Unnee Ranjan,
Viviana R Ramirez,
Wei Wang, PhD
Anna R Kwilas's Documents
Publish Date | Document Type | Title |
---|---|---|
February, 2021 | EIR | CELGENE CORPORATION - EIR, 2021-03-10 |
November, 2022 | FDA 483 | Krystal Biotech, Inc. - Form 483, 2022-11-16 |
February, 2021 | FDA 483 Response | CELGENE CORPORATION - Form 483R, 2021-03-11 |
February, 2021 | FDA 483 | CELGENE CORPORATION - Form 483, 2021-02-19 |
February, 2024 | FDA 483 | Resilience US, Inc. - Form 483, 2024-02-16 |
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