FDA Investigator Julie A Stocklin

Julie A Stocklin has conducted inspections on 15 sites in 1 countries as of 29 May 2002. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
15
Last Inspection Date:
29 May 2002
Investigator Role:
FDA Investigator
Redica ID:
100001211
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Julie A Stocklin:
Abby M Miller, Alan D Grupe, Amalia C Himaya, Annette L Diggs, Arie C Menachem, Arsen Karapetyan, Avery J Dennis, Babajide Michael Osunsanmi, Benjamin S Liao, Binh T Nguyen, Brenda K Alford, Brenda L Reihing, Brian J Ryan, Brien C Fox, Bruce R Burrell, Bryan A Galvez, Bryce E Mansfield, Camille Bennett Hoffman, Carla J Lundi, Caryn M Everly, Caryn M Mcnab, Cathleen A Carr Sharpe, CDR Rochelle B Young, RPh, MSA, Chelsea N Sealey, Christopher R Czajka, Christopher S Genther, Deborah A Greco, Deborah A Nebenzahl, Donna Mwilliams Hill, PhD, Gene D Arcy, Gerard Pde Leon, Greg K Keshishyan, Harmon M Blanch, Hugh A Grimoldby, Jade A Rorberg, James C Henry, James I Vik, Jamie M Du, Jane S Wernberg, Jeanne M Weishaar, Jeffrey N Gerdes, Jeffrey P Raimondi, Jennifer M Gogley, Jessica L Kocian, Jinkee Mvila Binayug, Joey V Quitania, John A Gonzalez, John W Banks, Jolanna A Norton, Jonathan T Little, Julia E Chervoni, Julie A Rorberg, Kari M Johansen, Katherine E Jacobitz, Katherine L Arnold, Kelley, Kelvin Cheung, Kelvin X Sanders, Kim Lthomas Cruse, Laurissa S Flowers, Leya A Grosch, Liming Zhang, Linda Thai, Ling Yu L Liu, Lisa A Bowden, Louis B Cencetti, Marcus F Yambot, Margo C Jones, Marijo B Kambere, PhD, Mark E Imsland, Mark E Moen, Mark S Crippen, Mark W Babbitt, Matthew J Johnson, Maxyne T Lam, Michael D Garcia, Michael J Donovan, Mihaly S Ligmond, Mikel T Wright, Nancy E Byerly, Nancy L Rolli, Nicholas L Hunt, Philip E Ake, Prasad Peri, PhD, Rebecca T Davis, Richard A Martin, Richard C Chiang, Rocco C Black, Ronald E Gill, Rumany C Penn, PharmD, S Lori Brown, PhD MPH, Saied A Asbagh, Sarah A Hassas, Scott W Fox, Selene T Torres, Sharon K Ferguson, Shelagh D Schopen, Shirnette D Ferguson, Stephanie A Slater, MS, Steven E Porter, Jr, Taichun Qin, PhD, Tajah L Blackburn, Tamala P Magee, Terri L Dodds, Thanh M Andrews, Thao T Kwan, Thomas C Mclean, CFS, Thomas J Arista, Uttaniti Limchumroon (Tom), Vickie L Anderson, Virgilio F Pacio, CSO, William C Hughes, Willis L Hicks, Yvonne M Larsen, Yvonne T Lacour, Zachary A Bogorad

Julie A Stocklin's Documents

Publish Date Document Type Title
June, 2001 FDA 483 Bachem Americas, Inc. - Form 483, 2001-06-08
August, 2000 EIR Gilead Sciences, Inc. - EIR, 2000-08-25
November, 2001 FDA 483 Response Bachem Americas, Inc. - Form 483R, 2001-11-27
December, 2000 FDA 483 Response Kindeva Drug Delivery L.P. - Form 483R, 2000-12-20
August, 2000 FDA 483 Response Gilead Sciences, Inc. - Form 483R, 2000-09-12
December, 2000 EIR Kindeva Drug Delivery L.P. - EIR, 2000-12-13
October, 2000 FDA 483 MD Pharmaceuticals aka Celltech Manufacturing - Form 483, 2000-10-24
June, 2001 EIR Bachem Americas, Inc. - EIR, 2001-06-08
November, 2000 FDA 483 S&B Pharma LLC dba Norac Pharma - Form 483, 2000-11-06
December, 2000 FDA 483 Kindeva Drug Delivery L.P. - Form 483, 2000-12-13
October, 2000 EIR MD Pharmaceuticals aka Celltech Manufacturing - EIR, 2000-10-24
November, 2001 FDA 483 Bachem Americas, Inc. - Form 483, 2001-11-27
August, 2000 FDA 483 Gilead Sciences, Inc. - Form 483, 2000-08-25
November, 2001 EIR Bachem Americas, Inc. - EIR, 2001-11-27

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