FDA Investigator Liliya R Robertson
Liliya R Robertson has conducted inspections on 1 sites in 1 countries as of 31 Jan 2022. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
1
Last Inspection Date:
31 Jan 2022
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Liliya R Robertson:
Adam M True,
Alexandra A Carrico,
Ana E Morales,
Anthony R Petriella,
Brian J Mundo,
Brittany A Mckenzie,
Christi L Bellmore,
Courtney E Hillier,
Crystal L Parks,
Daniel B Arrecis,
Danny Tuntevski,
Dariusz Galezowski,
David M Amy,
Donald W Myrick,
Elizabeth P Mayer,
Erin M Miller,
Geneve M Maxwell,
Geneve M Parks,
Jennifer R Johnson,
John N Woodall,
Kathryn G Brown,
Kelley L Clark,
Liliya V Bubiy,
Lisa M Thursam,
Logan M Ebeling,
Margaret N Persich,
Marlon K Turner,
Martha Sullivan Myrick,
Martin R Vowell,
Matthew R Buenconsejo,
Micmarie Ramos Rodriguez,
Nicholas E Boyd,
Robert G Taylor,
Rohn R Robertson,
Roshni J Patel,
Shana L Williams,
Theodore N Sietsema,
Tonnie L Carter,
Vera M Anderson,
Vesa Vuniqi,
William D Tingley
Liliya R Robertson's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2022 | FDA 483 | Abbott Laboratories - Form 483, 2022-03-18 |
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