FDA Investigator Christopher D Washington

Christopher D Washington has conducted inspections on 11 sites in 1 countries as of 12 Mar 2018. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
11
Last Inspection Date:
12 Mar 2018
Investigator Role:
FDA Investigator
Redica ID:
100002927
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Christopher D Washington:
Amalia C Himaya, Angela Shepas, Binh T Nguyen, Bryan A Galvez, Carrie A Hughes, Caryn M Mcnab, Cassandra L Abellard, Cathleen A Carr Sharpe, Cecilia H Kieu, Christopher M Jenner, Claudia Mperez Kasmarski, Darren S Brown, Darrin E Davis, Deborah A Greco, Diane Cvan Leeuwen, Dogbeda F Mackenzie, Donna Ltartaglino Besone, Francisco, Greg K Keshishyan, Gunneet Kaur, Henry E Carrillo, Herminio C Francisco, James R Fleckenstein, Janet Pulver, Jeffrey P Raimondi, Jennifer M Gogley, Joey V Quitania, Judy C Nepsa, Kari M Johansen, Kelley, Kelvin X Sanders, Kham Phommachanh, Lanita F Kelley, Leonard H Lavi, Liming Zhang, Linda Thai, Matthew R Clabeaux, Maxyne T Lam, Michael D Garcia, Mihaly S Ligmond, Natalie J Ayoub, Nianna C Burns, Phillip J Sample, Rabin N Ghoshal, Rafael A Kaup, Richard A Abate, Richmond K Yip, Rocio Guzman Velazquez, Saied A Asbagh, Sean P Desbrow, Shannon B Ruelle, Sonia R Peterson, Stacie A Woods, Stephanie A Slater, MS, Sumit Sen, Tara L Stockton, Truong Xuan Nguyen (Andy), Trushani T Desai, Uttaniti Limchumroon (Tom), Vashti E Bocker, Vioela J Caze, Virgilio F Pacio, CSO, Yen Tso Kuo, Yi Lin, Yumi J Hiramine, Yvonne T Lacour, Zachary A Bogorad

Christopher D Washington's Documents

Publish Date Document Type Title
December, 2017 FDA 483 Response bB BIOCHEM LABORATORIES INC. - Form 483R, 2018-01-09
June, 2017 FDA 483 Response Diasol Inc. - Form 483R, 2017-07-05
June, 2017 FDA 483 Diasol Inc. - Form 483, 2017-06-21
December, 2017 FDA 483 bB BIOCHEM LABORATORIES INC. - Form 483, 2017-12-18
October, 2017 FDA 483 Nexgen Pharma, Inc. - Form 483, 2017-10-20

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