FDA Investigator Ying Zhang
Ying Zhang has inspections in 1 countries as of 24 Jul 2023. Ying Zhang has collaborated with a combined 1068 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
3
Last Inspection Date:
24 Jul 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Amy L Singer,
Ankur C Patel,
Anna M Brannen,
Ariel Cruz Figueroa,
Arlene M Badillo,
Barbara Jwilimczyk Macri,
Bethany L Subel,
Byeongtaek Oh,
Christina Capacci Daniel, PhD,
Christopher T Middendorf,
Cynthia T Cain,
Edwin Martinez,
Elizabeth Ll Edwards,
Frederick Razzaghi,
German Rivera,
Jon P Antoniou,
Jorge L Guadalupe,
Jose Alopez Rubet,
Jose E Melendez, DDC,
Joshua P Wireman,
Kenneth E Felkley,
Krishna Ghosh, PhD,
Lareese K Thomas,
Lauren N Howard,
Lauren N Smith,
Laurimer Kuilan Torres,
Libia M Lugo,
Lindsey M Schwierjobann,
Lindsey M Schwierjohann,
Logan T Williams,
Marea K Harmon,
Margaret M Sands,
Marian E Ramirez,
Marianela Aponte Cruz,
Marianne Allen,
Mark E Parmon,
Michael P Sheehan,
Myriam M Sosa,
Nicholas L Paulin,
Noreen Muniz,
Paranthaman Senthamaraikannan,
Paul L Bellamy,
Ramon A Hernandez,
Rapti D Madurawe,
Raquel Gonzalez,
Raquel Gonzalez Rivera,
Rebecca Parrilla,
Rose Xu,
Russell J Glapion,
Steven P Eastham,
Tamil Arasu, PhD,
Tarun D Mehta,
Thomas J Arista,
Tracey L Harris,
Unnee Ranjan,
Vilmary Negron Rodriguez,
Wen Ning Chan (Sally)
Ying Zhang's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2017 | FDA 483 | Lilly del Caribe, Inc. - Form 483, 2017-07-21 |
February, 2015 | FDA 483 | CMIC CMO USA CORP - Form 483, 2015-02-13 |
February, 2015 | FDA 483 Response | CMIC CMO USA CORP - Form 483R, 2015-03-06 |
February, 2019 | FDA 483 | Patheon Pharmaceuticals Inc. - Form 483, 2019-02-15 |
February, 2019 | EIR | Patheon Pharmaceuticals Inc. - EIR, 2019-02-15 |
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