FDA Investigator William C Hughes
William C Hughes has conducted inspections on 155 sites in 1 countries as of 04 Jun 2007. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
155
Last Inspection Date:
04 Jun 2007
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 William C Hughes:
Aaron J Poloni,
Ali Kashani,
Alicia Aborg Borm,
Anita Narula, PhD,
Arie R Dyk,
Ashleigh P Barkans,
Barbara J Rincon,
Carol A Gripp,
Clint R Van Blaricom,
Connie P Rezendes,
Cynthia J Lee, MS,
Dandan Wang, PhD,
Devon M Shoop,
Dirk L Lincoln,
Don A Brunssen,
Donald B Mckechnie,
Elizabeth S Howell,
Emal Wahab,
Farhana Khan,
Gregory A Holt,
Harmon M Blanch,
Hughes,
Ian J Thomson,
Isaiah D Isakson,
James C Henry,
James D Hildreth,
James I Vik,
James S Stuart, BS,
Jeannine K Wooten,
Jeff A Gard,
Jeffrey J Leclair,
John E Emmert,
Julia Ventura,
Julie A Stocklin,
Katharine Chan,
Keegan B Mixon,
Kelsey M Bishop,
Kimberly Jproctor Jones,
Lance W Bohm,
Lisa K Capron,
Lori J Jennings,
Malinda C Shelman,
Marcus A Goshen,
Michael F Schuette,
Michael J Lackey,
Michael S Hudson,
Mihaly S Ligmond,
Mikel T Wright,
Nancy A Saxenian Emmons,
Nancy E Doyle,
Neil J Traaen,
Paul F Rader,
Paul M Kawamoto,
Peter T Regan,
Roger J Adams,
Ronald E Gill,
S Lori Brown, PhD MPH,
Sangeeta M Khurana, PhD,
Scott A Nabe,
Shannon J Hall,
Stephanie A Jameson,
Sunitha K Rajaram, PhD,
Thomas C Mclean, CFS,
Tracy K Li,
Wayne F Larson
William C Hughes's Documents
Publish Date | Document Type | Title |
---|---|---|
September, 2000 | EIR | The Veranda, P.C. - EIR, 2000-09-21 |
September, 2000 | EIR | Emerald Kalama Chemical, LLC - EIR, 2000-09-06 |
September, 2003 | EIR | West Coast Feed and Seed LLC - EIR, 2003-09-08 |
September, 2003 | EIR | Pacific Bio Products - Warrenton LLC - EIR, 2003-09-10 |
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