FDA Investigator Anthony J Grace
Anthony J Grace has conducted inspections on 35 sites in 3 countries as of 04 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
35
Last Inspection Date:
04 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
United Kingdom of Great Britain and Northern Ireland,
India
FDA Investigators that have inspected at least one site in common with Anthony J Grace:
Althea A Williams,
Amanda K Willey,
Ana P Barido,
Audrey J Yarbrough,
Barbara A Crowl,
Barbara D Wright,
Barbara M Frazier,
Betsy C Galliher,
Brandon L Mariner,
Brandy D Brown,
CDR Thomas R Berry, PPh,
Craig A Garmendia,
Cynthia A Harris, MD, RN,
Dana M Daigle,
Dana M Klimavicz,
David L Chon,
Donna D Gallien, MPH,
Eileen J Bannerman,
Erin L Mcfiren,
Erin M Mcdowell,
Gene R Gunn,
Jason D Abel,
Jawaid Hamid,
Joanne M Schlossin,
Jose Acruz Gonzalez,
Karen M Cooper,
Kip J Hanks,
Ladislav Kermet,
Latrice G Jones,
Laura L Staples,
Leon L Crawley,
Lillie D Witcher,
Lynda L Lanning,
Lynette P Salisbury,
Metitia G Sanders,
Metitia M Gramby,
Michelle D Haamid,
Natasha A Dezinna,
Nichole J Chamberlain,
Nicole M Bell,
Patricia S Smith,
Paul W Moy,
Randy L Clarida,
Reba A Gates,
Samantha J Pinizzotto, D V M,
Scott B Laufenberg,
Seneca D Toms,
Sheri S Oliver,
Stacey F Rivette,
Stephanie A Cochran,
Stephanie L Shapley,
Terri E Gibson,
Tracy R Ball,
Travis M Beard,
William P Tonkins
Anthony J Grace's Documents
Publish Date | Document Type | Title |
---|---|---|
April, 2024 | FDA 483 | John J. Wrenn, M.D. - Form 483, 2024-04-15 |
December, 2023 | FDA 483 | VA Medical Center IRB, W. G. (Bill) Hefner Salisbury - Form 483, 2023-12-07 |
April, 2024 | FDA 483 | WakeMed IRB - Form 483, 2024-04-29 |
October, 2022 | FDA 483 | Praveen Arla, D.O. - Form 483, 2022-11-01 |
July, 2024 | FDA 483 | State of Florida Department of Health IRB - Form 483, 2024-07-22 |
May, 2024 | FDA 483 | Integrated Laboratory Systems LLC, An Inotiv Company - Form 483, 2024-05-17 |
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