FDA Investigator Mildred J Tures
Mildred J Tures has conducted inspections on 24 sites in 1 countries as of 10 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
24
Last Inspection Date:
10 Jun 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 Mildred J Tures:
Benjamin W Anderson,
Carmen Y Fisher,
Christina L Bigham,
Denise L Burosh,
Douglas W Atkins,
James A Beaulieu,
Jennifer S Ness,
Jessica L Johnson,
Joseph D Gong,
Joseph M Edwin,
Kyle J Mccracken,
Marissa S Steinhagen,
Michelle J Glembin,
Nicole C Victoria, PhD,
Ralph Jerndal,
Ryan J Benedict,
Sharon L Matson,
Susan M Matthias,
Tony T Yang,
Traci C Kelm,
Tyler R Courtney,
Yehualashet A Gessesse
Mildred J Tures's Documents
Publish Date | Document Type | Title |
---|---|---|
May, 2022 | FDA 483 | rms Company - Form 483, 2022-05-18 |
September, 2023 | FDA 483 | APN Health LLC - Form 483, 2023-09-22 |
July, 2022 | FDA 483 | LISI MEDICAL Remmele, Inc - Form 483, 2022-07-12 |
April, 2022 | FDA 483 | Revolutionary Science - Form 483, 2022-04-06 |
November, 2022 | FDA 483 | Caerus Corp. dba Orthocor Medical - Form 483, 2022-11-22 |
April, 2023 | FDA 483 | LISI MEDICAL Remmele, Inc - Form 483, 2023-04-27 |
May, 2023 | FDA 483 | Dynamic Group, Inc - Form 483, 2023-05-31 |
April, 2024 | FDA 483 | Jessica A. Thomes-Pepin, M.D. - Form 483, 2024-04-08 |
January, 2024 | FDA 483 | Medspira, Llc - Form 483, 2024-01-16 |
October, 2024 | FDA 483 | George Hanson, M.D. - Form 483, 2024-10-03 |
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