FDA Investigator Clinton D Priestley
Clinton D Priestley has conducted inspections on 70 sites in 1 countries as of 20 Mar 2013. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
70
Last Inspection Date:
20 Mar 2013
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 Clinton D Priestley:
Aaron J Fox,
Allison E Sincek,
Amy L Mccarthy,
Andrew I Carr,
Andrew J Lang,
Annemarie E Hoffman,
Annemarie H Cochran,
Annemarie Kleiza,
Ashley R Karns,
Benjamin J Dastoli,
Benjamin P Stewart,
Brittany M Kershaw,
Carlos H Ruiz,
Catherine D Djordjevic,
Christopher D Snyder,
Craig P Seaborn,
Craig T Rybus,
Darla J Christopher,
Darren S Morgan,
Dell S Moller,
Diane M Fresch,
Diane R Mcdaniel,
Donald A Howell,
Dorathy M Eischen,
Dr. Abhijit Raha, PhD,
Dr. Mark J Seaton, PhD,
Dr. Zhou Chen (nmi), MD PhD,
Edward R Kay,
Emily E Krumel,
Frederick M Lochner,
Holly J Wilson,
Hugh M Mcclure, II,
Janet L Bowen,
Jeffrey A Sincek,
Jennifer A Downie,
Jennifer A Pruden,
Jennifer M Heitz,
John D Jaworski,
Karen M Cooper,
Karen M Kondas,
Katherine M Taylor,
Kathryn J Mccarty,
Keith J Mason, Jr,
Kimberly A Joseph,
Laureen M Geniusz,
Lisa M Marko,
LTJG Bradley E Benasutti,
Maney P Sturgill,
Marcia A Worley,
Mary E Storch,
Matthew H Pitts,
Michael E Campbell,
Michael E Clark,
Michael K Larson,
Mishelle L Harriger,
Nadeem I Chaudhry,
Nancy L Neiger,
Nicholas L Paulin,
Pifer,
Richard W Berning,
Said H Muse,
Shannon F Underwood,
Stephen G Mclane,
Stephen J Kilker,
Susan M Taylor,
Tammy M Phillips,
Teresa K Kastner,
Thomas B Smith,
Thomas J Prigge,
Thomas W Nojek,
Yiyue Zhang (nmi), PhD
Clinton D Priestley's Documents
Publish Date | Document Type | Title |
---|---|---|
February, 2011 | FDA 483 | Nature Pure LLC - Form 483, 2011-02-16 |
May, 2011 | EIR | The Cleveland Clinic Foundation - EIR, 2011-05-25 |
April, 2012 | FDA 483 | Frontage Laboratories, Inc. - Form 483, 2012-04-20 |
April, 2012 | FDA 483 Response | Frontage Laboratories, Inc. - Form 483R, 2012-05-04 |
April, 2012 | EIR | Frontage Laboratories, Inc. - EIR, 2012-04-20 |
January, 2012 | FDA 483 | Gebauer Company - Form 483, 2012-01-26 |
March, 2011 | FDA 483 | Clovervale Farms - Form 483, 2011-03-09 |
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