FDA Investigator Grace Deneke
Grace Deneke has conducted inspections on 2 sites in 1 countries as of 28 Mar 2011. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
2
Last Inspection Date:
28 Mar 2011
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 Grace Deneke:
Amir Alavi,
Ashley N Queen, PhD,
Burnell M Henry,
Carrie A Hughes,
Cassandra L Abellard,
Cathleen A Carr Sharpe,
Christian D Lynch (CDL),
Christopher R Czajka,
David G Whitman,
Destry M Sillivan,
Edward A Brunt,
Emmanuel A Dimaano, Jr,
Esther C Broner, PhD,
Gerald D Bromley, Jr,
Helen B Ricalde,
Jacqueline Mdiaz Albertini,
Jennifer M Gogley,
Joey V Quitania,
Joseph George,
Justin A Boyd,
Katherine E Jacobitz,
Lata C Mathew, PhD,
Laurimer Kuilan Torres,
Lestine C Webb,
Linda Thai,
Marion Michaelis,
Michael Shanks, MS,
Michael T Cyrus,
Nayan J Patel,
Nisha C Patel,
Omotunde O Osunsanmi,
Rebecca K Olin,
Santiago Gallardo Johnson,
Taichun Qin, PhD,
Thuy T Nguyen, LCDR,
Virgilio F Pacio, CSO,
Virginia Carroll, PhD,
Yi Wang, PhD
Grace Deneke's Documents
Publish Date | Document Type | Title |
---|---|---|
April, 2011 | FDA 483 | Ajinomoto Althea, Inc. - Form 483, 2011-04-01 |
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