FDA Investigator Lillian Mcolon Mcknight
Lillian Mcolon Mcknight has conducted inspections on 4 sites in 1 countries as of 22 Feb 2022. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
4
Last Inspection Date:
22 Feb 2022
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 Mcolon Mcknight:
Caroline Strasinger,
CDR Ileana Barreto Pettit,
Cheryl A Clausen,
Christie A Soto,
Christos G Tsingelis,
Dr. Ralph M Bernstein, PhD,
Gregory Price,
Jennifer L Bridgewater,
Jennifer Lalama,
Jennifer M Menendez,
Jessica L Pressley,
Joanne E King,
Jose Velez,
Joshua J Silvestri,
Kayla V Sprague,
Larry K Hampton,
Laura Fontan, MS,
LCDR Michael H Tollon,
LT Richard A Lyght,
Megan T Ziegler,
Mizanne E Lewis,
Naveen B Kanthamneni,
Noreen Muñiz,
Philippa Hillyer,
Robert C Coleman,
Roy R Rinc,
Salvatore N Randazzo,
Sarah E Mcmullen,
Sarah Ibrahim,
Scott T Ballard,
Steven D Dittert,
Suzanne N Vallez,
Victor Spanioli,
Virginia L Meeks,
Vivin George,
Yifan Wang
Lillian Mcolon Mcknight's Documents
Publish Date | Document Type | Title |
---|---|---|
November, 2021 | FDA 483 | Noven Pharmaceuticals, Inc. - Form 483, 2021-11-17 |
February, 2022 | FDA 483 Response | MOHNARK PHARMACEUTICALS INC. - Form 483R, 2022-03-08 |
October, 2021 | FDA 483 | Lonza Tampa LLC - Form 483, 2021-10-01 |
February, 2022 | FDA 483 | MOHNARK PHARMACEUTICALS INC. - Form 483, 2022-02-25 |
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