FDA Investigator Gary L Zaharek

Gary L Zaharek has conducted inspections on 217 sites in 2 countries as of 18 Mar 2010. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
217
Last Inspection Date:
18 Mar 2010
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America, Canada
FDA Investigators that have inspected at least one site in common with Gary L Zaharek:
Abraham M Maekele, Alla Dubrovsky, Althea A Williams, Amogh Pathi, Anderson, Andrea P Scott, Anthony E Keller, RPh, Barbara J Moynier, Brenda L Reihing, Brittany D Mccracken, Calvin K Cook, Catherine J Laufmann, Christine M Parmentier, Christopher S Genther, Daniel C Geffin, Deborah A Nebenzahl, Dennis G Kawabata, Dennis R Butcher, Dolores Harper, Don A Leeseberg, Dustin R Abaonza, Emir Galevi, Eric J Heinze, Eric M Padgett, Eric W Anderson, Finn A Slizza, Francis J Eng, Frank P Bianco, James A Lane, James D Hildreth, James E Frye, James W Whitney, Jeff A Gard, Jeffrey W Shrifter, DPM, Jinkee Mvila Binayug, Jocelyn E Massey, Jocelyn T Ramos, John A Hall, John A Sciacchitano, John E Emmert, Jolene S Hedgecock, Joseph A Seitz, III, Juan A Morales, Jude C Dikes, Karen D Phung, Kellie L Thommes, RN, Kham Phommachanh, Kimberly L Anderson, Kimberly L Pruszko, Kimberly Lewandowski Walker, Kingj, Laverne Kimble, Lawton W Lum, Leo J Lagrotte, Linda Linh N Adams, Linda S Shook, Lori J Silverstein, Lorna F Jones, LT Mark A Chen, MPH, Lydia S Chan, Maida Henesian (NMI), Mark E Chan, Marlo Ianm Alintanahin, Mary R Hole, Matthew A Walburger, Miaja Umaedi, Nancy A Saxenian Emmons, Paul M Kawamoto, Philip E Ake, Phillip M Pontikos, Quynh H Strandberg, Rebecca L Stephany, Rosanna M Goodrich, Ruark Lanham, Samuel K Gibbons, Jr, Scott A Nabe, Seema S Singh, Selene T Torres, Sergio Chavez (NMI), Sherri N Rohlf, MD, Stanley B Eugene, BS, BME, Stuart W Russell, Suzie L Kent, Tamara S Rosbury, Timothy C Grome, Trang N Cox, Vanessa R Muller, Xiaojun Yan, Yvette Mlacour Davis

Gary L Zaharek's Documents

Publish Date Document Type Title
April, 2000 FDA 483 SDL, Inc - Form 483, 2000-04-14
November, 2002 FDA 483 Lumenis Inc. - Form 483, 2002-11-25
April, 2005 EIR HDC Corporation - EIR, 2005-04-13
November, 2003 FDA 483 New Wave Research Division of esi - Form 483, 2003-11-19
December, 2001 EIR Abbott Laboratories - EIR, 2001-12-17
October, 2003 FDA 483 Laser Reference - Form 483, 2003-10-29
August, 2003 FDA 483 Sunrise Telecom Inc - Form 483, 2003-08-27
June, 2001 EIR MML Diagnostics Packaging, Inc - EIR, 2001-06-12
December, 2001 FDA 483 Abbott Laboratories - Form 483, 2001-12-17
November, 2003 EIR New Wave Research Division of esi - EIR, 2003-11-19
July, 2007 EIR VISX INCORPORATED, A SUBSIDIARY OF AMO INC - EIR, 2007-07-31
July, 2007 FDA 483 VISX INCORPORATED, A SUBSIDIARY OF AMO INC - Form 483, 2007-07-31
September, 2009 FDA 483 Cardiva Medical, Inc. - Form 483, 2009-09-03
September, 2009 FDA 483 Siemens Industry Inc - Form 483, 2009-09-15
April, 2001 FDA 483 Semler Technologies Inc - Form 483, 2001-04-24
December, 2005 EIR Nidek, Inc. - EIR, 2005-12-15
October, 2003 EIR Laser Reference - EIR, 2003-10-29
August, 2003 FDA 483 Onetta, Inc. - Form 483, 2003-08-20
December, 2002 FDA 483 Molecular Devices Corp. - Form 483, 2002-12-04
April, 2001 FDA 483 Response Semler Technologies Inc - Form 483R, 2001-05-21
April, 2001 EIR Semler Technologies Inc - EIR, 2001-04-24
August, 2003 EIR Sunrise Telecom Inc - EIR, 2003-08-27
May, 2007 FDA 483 Illumina, Inc. - Form 483, 2007-05-18
April, 2005 FDA 483 HDC Corporation - Form 483, 2005-04-13
June, 2001 FDA 483 Response MML Diagnostics Packaging, Inc - Form 483R, 2001-07-11
June, 2001 FDA 483 MML Diagnostics Packaging, Inc - Form 483, 2001-06-12

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