FDA Investigator Kimetha A King
Kimetha A King has conducted inspections on 44 sites in 1 countries as of 03 Aug 2010. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
44
Last Inspection Date:
03 Aug 2010
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 Kimetha A King:
Alan P Kurtzberg,
Althea A Williams,
Amanda S Zorn,
Andrew M Kolenc,
Ashleigh P Barkans,
Ashleigh P Wodushek,
Azotearc,
Bryan J Love,
Chelsea N Sealey,
Christine I Shaw,
Daniel J Lahar,
Debra L Curtis,
Dolores Harper,
Dustin M James,
Erika V Butler,
Felix J Marrero,
Frank L Cordova,
Genoula K Ryan,
Ginger M Sykes,
Grace E Mcnally,
Hanna L Potter,
James R Montero,
Jamie L Dion,
Janet Pulver,
John Diehl,
Jonathan R Campos,
Justin H Erickson,
Kathleen S Tormey,
Keith C Littrell,
Kristen E Szenderski,
Lori A Carr,
Lori A Lahmann,
Manuel A Moreno,
Marc A Jackson, Jr,
Martina E Lagrange,
Matthew M Vernon,
Matthew R Dionne,
Michael J Kuchta,
Michael R Goga,
Michelle D Motsinger,
Nathan M Jornod,
Nicholas R Nance,
Patricia A Maestas,
Philip E Ake,
Ricki A Chase,
Shererk,
Steve P Yost,
Teena H Aiken,
Thai T Duong,
Theressa B Smith,
Tuan A Nguyen,
Vicky L Cruz,
Vivian Garcia,
Zachary L Miller,
Zachary L Stamm
Kimetha A King's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| August, 2010 | FDA 483 | BioFire Diagnostics, LLC - Form 483, 2010-08-05 |
| February, 2010 | FDA 483 | Koko, LLC - Form 483, 2010-02-09 |
| December, 2009 | FDA 483 | Encision Inc. - Form 483, 2009-12-11 |
| March, 2009 | EIR | ARCA biopharma, Inc. - EIR, 2009-03-09 |
| November, 2007 | FDA 483 | VIBE Technologies - Form 483, 2007-11-16 |
| March, 2009 | FDA 483 Response | ARCA biopharma, Inc. - Form 483R, 2009-04-03 |
| April, 2010 | FDA 483 | Septodont, Inc - Form 483, 2010-04-14 |
| March, 2009 | FDA 483 | ARCA biopharma, Inc. - Form 483, 2009-03-09 |
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