FDA Investigator Christopher K Gibbs
Christopher K Gibbs has conducted inspections on 32 sites in 1 countries as of 11 Mar 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
32
Last Inspection Date:
11 Mar 2024
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 Christopher K Gibbs:
Adam C Hipko,
Alanna L Mussawwir Bias,
Alcee M Tavarez,
Angela Mock,
Anh M Lac,
Anya Dlockett Evans,
Bing Lin,
Blondell W Johnson,
Brandon K Barbee,
Brenda G Stewart Munoz,
Brook Shea,
Chad J Whitwell,
Charles D Brown,
Christopher D Rush,
Christopher J Hurst,
Cindy J Jeffrey,
Cymbre Weatherly,
Dallas E Gilbreath Jr,
Dana M Lewis,
Daniel J Lahar,
Daniel S Fam,
Danielle Lyke,
Danny D Horner,
Denise Connelly,
Deniza Karacic,
Ed Gonzalez Vazquez,
Elisa M Fleming,
Erick G Marchan,
Ernest Serna, III,
Fernando C Martinez,
Frans E Mercado,
Gatica,
Gery M Duparc,
Grant L Davis,
J Elkins,
Jacob W Reynolds,
Jamie M Bumpas,
Janice M Hickok,
Jeffrey R Wooley,
Jennifer O Dowdy,
Jeremy L Stukes,
Jodi M Gatica,
Johnson,
Jonathan A Womack,
Jonathan M Mcbride,
Juan D Lopez,
Karlton T Watson,
Kathleen Chmura Shaffer,
Kayla R Deatherage,
Kenitra D Hewitt,
Kunapuli T Madhusudhan,
L Grant,
Lauren E Skokan,
Lauren R Brady,
Lisa M Puttonen,
Lisa R Jennings,
Liza L Quiles,
Lorie S Hannappel,
Margarito J Uribe,
Martha S Baldwin,
Micmarie Ramos Rodriguez,
Monique Rac Lester,
Monique S Frazier,
Nilantha Bandara,
Pauline N Logan,
Payne,
Philip M Steele, PhD,
Phillip J Sample,
Pitman,
Quynh Anh H Tran,
Rebecca Co Bryan,
Robert T Harris,
Samuel A Hamblin,
Sandy J Ziegler,
Seri L Essary,
Tamera H Hunt,
Tara A Gray,
Toby Vern H Hill,
Travis S Brown,
Trina K Vick,
Verlinda A Narcisse,
Yaw O Osei,
Young M Yoon,
Zumera B Ajani
Christopher K Gibbs's Documents
Publish Date | Document Type | Title |
---|---|---|
June, 2012 | FDA 483 | Coca-Cola Refreshments USA, Inc. - Form 483, 2012-06-05 |
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](https://redica.com/document-store/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