FDA Investigator Julie A Rorberg
Julie A Rorberg has conducted inspections on 5 sites in 1 countries as of 13 Nov 2001. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
5
Last Inspection Date:
13 Nov 2001
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Julie A Rorberg:
Amalia C Himaya,
Arie C Menachem,
Arsen Karapetyan,
Babajide Michael Osunsanmi,
Benjamin S Liao,
Binh T Nguyen,
Brian J Ryan,
Brien C Fox,
Bryan A Galvez,
Carla J Lundi,
Caryn M Everly,
Caryn M Mcnab,
Cathleen A Carr Sharpe,
CDR Rochelle B Young, RPh, MSA,
Chelsea N Sealey,
Deborah A Greco,
Donna Mwilliams Hill, PhD,
Greg K Keshishyan,
Jamie M Du,
Jane S Wernberg,
Jeffrey P Raimondi,
Jennifer M Gogley,
Joey V Quitania,
John A Gonzalez,
Julie A Stocklin,
Kari M Johansen,
Katherine E Jacobitz,
Kelley,
Kelvin Cheung,
Kelvin X Sanders,
Kim Lthomas Cruse,
Liming Zhang,
Linda Thai,
Ling Yu L Liu,
Louis B Cencetti,
Marcus F Yambot,
Matthew J Johnson,
Maxyne T Lam,
Michael D Garcia,
Mihaly S Ligmond,
Nancy L Rolli,
Nicholas L Hunt,
Prasad Peri, PhD,
Richard C Chiang,
Rumany C Penn, PharmD,
Saied A Asbagh,
Sarah A Hassas,
Selene T Torres,
Shirnette D Ferguson,
Stephanie A Slater, MS,
Steven E Porter, Jr,
Taichun Qin, PhD,
Tajah L Blackburn,
Tamala P Magee,
Terri L Dodds,
Thao T Kwan,
Thomas J Arista,
Uttaniti Limchumroon (Tom),
Vickie L Anderson,
Virgilio F Pacio, CSO,
Yvonne T Lacour,
Zachary A Bogorad
Julie A Rorberg'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 |
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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