FDA Investigator Shelley L Waring

Shelley L Waring has conducted inspections on 26 sites in 1 countries as of 05 Nov 2002. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
26
Last Inspection Date:
05 Nov 2002
Investigator Role:
FDA Investigator
Redica ID:
100003779
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Shelley L Waring:
Albert A Salvador, Amanda B Athey, Anita R Michael, Ann Marie Karnick, Ann Marie Montemurro, Ann Marie Schofield, Anne E Johnson, Brandon J Brookens, Brandon M Kurjanowicz, Burnell M Henry, Calvin W Edwards, Cara M Minelli, Carl E Lovrich, CDR Michael J Mero, Chamberlain, Christina K Theodorou, Daniel J Mechenbier, David J Hafner, David J Hapner, David L Pearce, Dawn D Aiello, Debra L Pagano, Erica L Nicoll, Erik A Bungo, Erika M Wilkerson, Gayle S Lawson, George Pyramides, James C Maclaughlin, James P Mcevoy, James R Evans, Javier E Santos, Joseph L Despins, PhD, Joseph T Dougherty, Judith A Paterson, Julianne C Mccullough, Junho Pak, Katelyn Astaub Zamperini, Kelly N Kerr, Kimberly A Dux, LCDR Margaret Edi Gennaro, LCDR Susan E Polifko, Linda M Hoover, Lisa M Bellows, Lisa M Feola, LT John M Mastalski, LTJG Bradley E Benasutti, Luella J Rossi, Luis A Dasta, Marlene L Davis, Marsha W Major, Maureen A Wentzel, Megan M Lauff, Michael A Taylor, Michele M Falchek, Myrick, Nikisha M Bolden, Nisha C Patel, Prabhu P Raju, Rachael O Oyewole, Robert B Shibuya, MD, Robert Jennings, Ronald A Stokes, Ronald T Colucci, Sean Y Kassim, PhD, Shusheen A Alexander, Stephanie Mangigian, MS/OSH, RN, Susan F Laska, MS, Tammy L Chavis, Thomas E Friel, Timothy J Schmidt, Todd J Maushart, Travis R Hunt

Shelley L Waring's Documents

Publish Date Document Type Title
February, 2000 FDA 483 Corixa Corporation - Form 483, 2000-02-17
May, 2000 EIR Eurofins Lancaster Laboratories, Inc - EIR, 2000-05-03
February, 2000 EIR Corixa Corporation - EIR, 2000-02-17
February, 2000 FDA 483 Response Corixa Corporation - Form 483R, 2000-05-03

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