FDA Investigator Jeffery A Johnson
Jeffery A Johnson has conducted inspections on 9 sites in 1 countries as of 14 Feb 2017. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
9
Last Inspection Date:
14 Feb 2017
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 Jeffery A Johnson:
Abby M Miller,
Adam R Cooke,
Alan P Kurtzberg,
Amanda L Fyles,
Amir Alavi,
Andrew S Limson,
Anita Narula, PhD,
Armando Chavez, MS,
Babajide Michael Osunsanmi,
Bichsa T Tran,
Binh T Nguyen,
Bruce R Burrell,
Bryan A Galvez,
Calvin B Koerner,
Camille Bennett Hoffman,
Carla J Lundi,
Caryn M Everly,
Caryn M Mcnab,
Christopher M Jenner,
Comyar Shoghi,
Darren S Brown,
David A Quale,
Diana M Rand,
Dyana K Stone,
Emanual A Kahsai,
Erica R Mahone,
Frederick L Fricke,
Gabriel Craig,
Gina C Collins,
Gregory A Berg,
Harmon M Blanch,
Heika R Tait,
Ian J Thomson,
James E Trabert,
Janet D Blount,
Jeanne M Weishaar,
Jennifer M Gogley,
Joe X Phillips,
Joey V Quitania,
John A Gonzalez,
Jonathan T Little,
Joseph X Phillips,
Katharine Chan,
Katherine E Jacobitz,
Kham Phommachanh,
Kim Lthomas Cruse,
LCDR Ismael Olvera, IV,
Lenita R Silvera,
Linda F Murphy,
Lisa A Bowden,
Marco S Esteves,
Marcus F Yambot,
Margo C Jones,
Mariza M Jafary,
Marsha L Mccauley,
Michael D Garcia,
Mihaly S Ligmond,
Mikel T Wright,
Minh D Phan,
Omotunde O Osunsanmi,
Prabhu P Raju,
Randall N Johnson,
Raymond T Oji,
Richard A Martin,
Richmond K Yip,
Sangeeta M Khurana, PhD,
Santiago Gallardo Johnson,
Scott W Fox,
Selene T Torres,
Shannon B Ruelle,
Sonia R Peterson,
Sparky L Bartee,
Tamala P Bogan,
Tamala P Magee,
Terri L Dodds,
Thao T Kwan,
Thomas C Mclean, CFS,
Thomas J Arista,
Timothy T Kapsala,
Truong Xuan Nguyen (Andy),
Uttaniti Limchumroon (Tom),
Vashti E Bocker,
Virgilio F Pacio, CSO,
Walden H Lee,
Yumi J Hiramine,
Zachary A Bogorad
Jeffery A Johnson's Documents
Publish Date | Document Type | Title |
---|---|---|
June, 2016 | FDA 483 | P & L Development, LLC - Form 483, 2016-06-24 |
September, 2016 | FDA 483 | Island Kinetics, Inc. d.b.a. CoValence Laboratories - Form 483, 2016-09-02 |
October, 2016 | FDA 483 | New Era Pharmacy, LLC - Form 483, 2016-10-04 |
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