FDA Investigator Tania E Garcia

Tania E Garcia has conducted inspections on 14 sites in 2 countries as of 07 Dec 2009. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
14
Last Inspection Date:
07 Dec 2009
Investigator Role:
FDA Investigation Participant
Redica ID:
100002781
Countries of Inspections:
United States of America, Canada
FDA Investigators that have inspected at least one site in common with Tania E Garcia:
Alberto A Viciedo, Amy M Cramer, Andrew A Leboeuf, Brian S Keefer, Byungja E Marciante, Catherine J Laufmann, Christina N Maurino, Christine M Cerenzio, Daniel J Grabicki, David H Smith, Deborah B Nixon, Denise M Visco, Investigator, Douglas C Kovacs, Dr. Sriram Subramaniam, PhD, Edward D Mcdonald, Emily A Walters, Eric J Cunningham, Eric Rothschild, Erin D Mccaffery, Frank J Marciniak, Frederick F Razzaghi, Gale L Glinecki, Gregson A Joseph, Helen Verdel, Jacqueline S Warner, James W Leonette, Jamie D Richardson, Jamie D Swann, Jean M Kelahan, Jeffrey J Ebersole, Joseph F Mcginnis, RPh, Karen E D'orazio, Keith M Reilly, Kelli F Dobilas, Kimberly Lewandowski Walker, Kinh Q Mac, Kristina L Conroy, Laureen M Geniusz, Laurissa S Flowers, Li Li, Lisa Harlan, Lori S Lawless, Meredith L Sheridan, Michael R Klapal, Monika Borkowska, Nancy F Scheraga, Nebil A Oumer, Paul L Bellamy, Rachel C Harrington, Richard H Penta, Robert G Ruff, Sarah Forney, Shirley H Isbill, Sinai I Davis, Tania E Vizcaino, Tara G Bizjak, Tara R Gooen, Thomas N Adjabeng, Toniette K Williams, Walter L Fava, William R Chang, Yehualashet A Gessesse, Yvesna C Blaise, Zakaria I Ganiyu

Tania E Garcia's Documents

Publish Date Document Type Title
August, 2003 EIR EUROMED, INC. - EIR, 2003-08-01
March, 2004 EIR Health Tech Inc - EIR, 2004-03-10
January, 2006 FDA 483 AJP Scientific, Inc. - Form 483, 2006-01-26
December, 2002 EIR Nelson Laboratories Fairfield Inc. - EIR, 2002-12-09
March, 2004 FDA 483 Health Tech Inc - Form 483, 2004-03-10
September, 2003 EIR Viant Medical, Inc. - EIR, 2003-09-30
September, 2009 FDA 483 Tishcon Corporation - Form 483, 2009-09-03
September, 2002 EIR J&J Pharmaceutical Research & Development, L.L.C. - EIR, 2002-09-13
September, 2004 EIR Johnson & Johnson Consumer Companies, Inc. - EIR, 2004-10-12
August, 2003 FDA 483 EUROMED, INC. - Form 483, 2003-08-01
June, 2002 FDA 483 Response Ivax Pharmaceuticals Inc - Form 483R, 2002-07-10
May, 2003 FDA 483 Advanced Biomaterial Systems, Inc. - Form 483, 2003-05-08
September, 2002 FDA 483 J&J Pharmaceutical Research & Development, L.L.C. - Form 483, 2002-09-13
December, 2002 FDA 483 Nelson Laboratories Fairfield Inc. - Form 483, 2002-12-09
September, 2003 EIR QFIX - EIR, 2003-09-22
June, 2002 FDA 483 Ivax Pharmaceuticals Inc - Form 483, 2002-06-20
August, 2003 FDA 483 Response EUROMED, INC. - Form 483R, 2003-10-07
December, 2009 FDA 483 Medtronic CryoCath LP - Form 483, 2009-12-10
September, 2009 FDA 483 Tishcon Corporation - Form 483, 2009-09-03
August, 2003 EIR Depuy North Brunswick - EIR, 2003-08-26
September, 2003 FDA 483 QFIX - Form 483, 2003-09-22
June, 2002 EIR Ivax Pharmaceuticals Inc - EIR, 2002-06-20
September, 2002 FDA 483 Response J&J Pharmaceutical Research & Development, L.L.C. - Form 483R, 2002-09-20
May, 2003 EIR Advanced Biomaterial Systems, Inc. - EIR, 2003-05-08

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