FDA Investigator Tiana M Mckinley
Tiana M Mckinley has conducted inspections on 30 sites in 1 countries as of 08 May 2012. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
30
Last Inspection Date:
08 May 2012
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 Tiana M Mckinley:
Anthony D Peterson,
Barbara D Wright,
Bonnie E Conley,
Bonnie E Pierson,
Brian S Lynch,
Carolyn E Barney,
Casey L Hamblin,
Charles N Dupont,
Cherie T Parker,
Cheryl G Scott,
Cheryl L Watson,
Christopher J Adams,
Claude L Brunson,
Cody D Rickman,
Comyar Shoghi,
Cynthia L Bolte,
Cynthia L Medlin,
Dana M Klimavicz,
Danielle M Maddox,
Dolores E Price,
Donna D Gallien, MPH,
Doretha M Tonkins,
Doretha M Wilson,
Dylan R Jock,
Eddie J Rigsby,
Edward A Brunt,
Elizabeth D Connell,
Emily E Smith,
Erica M Katherine,
Francis A Guidry,
James W Blakely,
Jean A Peeples,
Jessica A Stephens,
Juanelma H Palmer,
June P Page,
Ka L Wong,
Karen Gale Sego,
Kari L Batey,
Kate E Jesse,
Katherine A Indingaro,
Kenneth R Merritt,
Kimberly D Tucker,
Kimberly J Hoffmeister,
Konsuela Y Glass,
Laressa R Gray,
Laura E Garcia,
Laura L Staples,
Lawrence A Butler,
LCDR Randall L Morris,
Leena Thomas,
Llopis,
M A Abel I,
Mark W Rivero,
Markeesa M Scales,
Marlene L Davis,
Mary A Millner,
Melanie L Drayton,
Michael T Nehring,
Nikki S Bryant,
Phillip A Driskell,
Randy D Baxter,
Richard J Bashay,
Richard L Garcia,
Samantha J Bradley,
Sandy L Atkins,
Shirhonda D Thorn,
Sidney M Smith,
Stephanie A Cochran,
Tammara D Perry,
Thomas B Smith,
Thomas O Morgan,
Tony E Bable,
Traci M Armand,
Whitney M White,
William D Bassett, Jr,
William P Chatham
Tiana M Mckinley's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2011 | EIR | Louisiana State University Health Sciences Center-Shreveport IRB - EIR, 2011-07-01 |
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