FDA Investigator Heika R Bounds
Heika R Bounds has conducted inspections on 2 sites in 1 countries as of 19 Jun 2008. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
2
Last Inspection Date:
19 Jun 2008
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Heika R Bounds:
Alexander M Kay,
Andrew R Wasko,
Anita Narula, PhD,
Ashar P Parikh,
Astrida B Mattson,
Barbara Janine Breithaupt,
Bradley Dworak, PhD,
Carl A Anderson,
Caryn M Mcnab,
Charles R Bonapace, PhD,
Christian D Lynch (CDL),
Christine A Harman, PhD,
Connie P Rezendes,
Ct Viswanathan, PhD,
Cynthia J Lee, MS,
Dawn E Barkans,
Dolores E Price,
Don H Bark, PhD,
Donald B Mckechnie,
Dr. Mark J Seaton, PhD,
Dr. Zhou Chen (nmi), MD PhD,
Dylan D Yao, MD, PhD,
Edwin Melendez,
Eileen A Liu,
Erin M Mcdowell,
Gerard Pde Leon,
Gloria J Baca, MS,
Grace P Santos,
Heika R Tait,
Hugh M Mcclure, II,
Jacqueline A O'shaughnessy, PhD,
Jacqueline Mdiaz Albertini,
Jane M Kreis,
Jennifer L Bridgewater,
Joey V Quitania,
Julian C Hanson,
Kari M Johansen,
Kathryn A Krentz,
Kenneth O Gee, PhD,
Kristin M Abaonza,
Laurel A Beer,
LCDR Debra Emerson,
Linda S Leja,
Lisa K Capron,
Lori J Silverstein,
Lynda L Perry, PhD,
Maria Pkelly Doggett, MBA,
Marijo B Kambere, PhD,
Mariza M Jafary,
Mark W Babbitt,
Maxine H Wong,
Michael F Skelly, PhD,
Mihaly S Ligmond,
Mikel T Wright,
Omotunde O Osunsanmi,
Paula A Trost,
Prabhu P Raju,
Randy L Self,
Rebecca Rodriguez,
Robert D Tollefsen,
S Lori Brown, PhD MPH,
Sangeeta M Khurana, PhD,
Sangeeta M Rataul,
Sunitha K Rajaram, PhD,
Susan F Laska, MS,
Terri L Dodds,
Thomas J Arista,
Tina S Roecklein,
Tracy K Li,
Uttaniti Limchumroon (Tom),
Xiomara Copeland
Heika R Bounds's Documents
Publish Date | Document Type | Title |
---|---|---|
October, 2002 | EIR | Altasciences Preclinical Seattle, LLC - EIR, 2002-10-11 |
July, 2008 | FDA 483 Response | Jubilant HollisterStier LLC - Form 483R, 2008-08-25 |
July, 2008 | FDA 483 | Jubilant HollisterStier LLC - Form 483, 2008-07-02 |
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