FDA Investigator John A Hall
John A Hall has conducted inspections on 21 sites in 1 countries as of 26 Dec 2003. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
21
Last Inspection Date:
26 Dec 2003
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 John A Hall:
Abraham M Maekele,
Alicia Aborg Borm,
Althea A Williams,
Beverly A Thomas,
Brenda K Alford,
Brenda L Reihing,
Bruce R Burrell,
Calvin K Cook,
Camille Bennett Hoffman,
Ce'nedra M Martin,
Colleen M Jones,
Cynthia L Gorveatt,
Dawn E Barkans,
Deborah A Nebenzahl,
Dennis G Kawabata,
Dirk L Lincoln,
Dolores Harper,
Don A Brunssen,
Don A Leeseberg,
Donald B Mckechnie,
Elizabeth A Sheller,
Emmanuel A Dimaano, Jr,
Gary L Zaharek,
George T Allen, Jr,
Gerald T O'connor,
Herbert E Arden,
Hugh A Grimoldby,
Hughes,
Ian J Thomson,
Jaclyn N Munsch,
Jacqueline M Bowling,
James D Hildreth,
Jeanne M Weishaar,
Jeff A Gard,
Jeffrey A Sincek,
Jocelyn T Ramos,
John E Emmert,
John Hall,
Jonathan T Little,
K Gonzlez,
Kelsey M Bishop,
Kimberly Jproctor Jones,
Leon R Marquart,
Lisa A Bowden,
Lori J Silverstein,
Lorna F Jones,
Marcus A Goshen,
Margaret A Foster,
Margo C Jones,
Mark E Moen,
Michael E Cimaglio,
Mikel T Wright,
Minh D Phan,
Msdap Gonzlezk,
Paula J Wilkerson,
Peter T Regan,
Philip E Ake,
Rebecca T Davis,
Sarah L Clark,
Scott A Nabe,
Sharon I Gundersen,
Stanley B Eugene, BS, BME,
Stephen R Souza,
Suzie L Kent,
Terri L Jones,
Xiaojun Yan
John A Hall's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2003 | EIR | Cascade Medical Center - EIR, 2003-08-26 |
April, 2001 | FDA 483 | Semler Technologies Inc - Form 483, 2001-04-24 |
April, 2001 | FDA 483 Response | Semler Technologies Inc - Form 483R, 2001-05-21 |
April, 2001 | EIR | Semler Technologies Inc - EIR, 2001-04-24 |
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