FDA Investigator Ve Garcia
Ve Garcia has conducted inspections on 11 sites in 2 countries as of 19 Apr 2004. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
11
Last Inspection Date:
19 Apr 2004
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America,
China
FDA Investigators that have inspected at least one site in common with Ve Garcia:
Althea A Williams,
Cynthia A Harris, MD, RN,
Daniel J Lahar,
Daniell Gill, Jr,
Danny D Horner,
David M Beltran,
Dolores Harper,
Ernest Serna, III,
Gregson A Joseph,
J Elkins,
Janete F Guardia,
Jerry Lott,
Jocelyn C Turner,
Johann M Fitch,
Joshua J Silvestri,
K Gonzlez,
Karen A Coleman,
Kelly J Pegg,
Marc R Dickens,
Monica J Wilkins,
Msdap Gonzlezk,
Pauline N Logan,
Richard K Vogel,
Shaquenta Y Perkins,
Vivian Garcia
Ve Garcia's Documents
| Publish Date | Document Type | Title |
|---|---|---|
| February, 2002 | EIR | Isomedix Operations, Inc. - EIR, 2002-02-20 |
| August, 2003 | EIR | Medtronic Sofamor Danek Usa, Inc - Dallas Distribution - EIR, 2003-08-06 |
| June, 2001 | EIR | Robert M Hardaway, III, Md - EIR, 2001-06-05 |
| March, 2000 | EIR | Clinipad Corp - EIR, 2000-03-16 |
| April, 2004 | EIR | Zhejiang Kindly Medical Devices Co., Ltd. - EIR, 2004-04-22 |
| December, 2000 | FDA 483 | Tekna Manufacturing, LLC - Form 483, 2000-12-14 |
| June, 2001 | FDA 483 | Texas Tech Univ Health Sciences Ctr-El Paso-MOBILE - Form 483, 2001-06-05 |
| December, 2003 | EIR | Changzhou Primed Medical Products Co., Ltd. - EIR, 2003-12-10 |
| May, 2000 | EIR | Alan Menter, MD/Clin Inv - EIR, 2000-05-29 |
| December, 2003 | FDA 483 | Holymed Products Co., Ltd. - Form 483, 2003-12-10 |
| April, 2002 | EIR | Medi Flex Hospital Products Inc - EIR, 2002-04-19 |
| April, 2004 | FDA 483 | Zhejiang Kindly Medical Devices Co., Ltd. - Form 483, 2004-04-22 |
| December, 2000 | EIR | Tekna Manufacturing, LLC - EIR, 2000-12-14 |
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