FDA Investigator Vipulchandra N Dholakia
Vipulchandra N Dholakia has conducted inspections on 4 sites in 2 countries as of 29 Feb 2016. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
4
Last Inspection Date:
29 Feb 2016
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America,
Switzerland
FDA Investigators that have inspected at least one site in common with Vipulchandra N Dholakia:
Andrew J Barrowcliff,
Andrew O Ejiofor,
Angela E Glenn,
Benjamin J Dastoli,
Brian D Rogers,
Brooke K Higgins,
Brooke K Seeman,
Bryce A Hammer,
Carole L Jones,
Charles C Conn, III,
Chiaochun J Wang,
Christopher T Middendorf,
Colleen F Hoyt,
Dell S Moller,
Diane T Bargo,
Diane T O'brien,
Djamila Harouaka,
Edmund F Mrak, Jr,
Edwin Melendez,
Emest F Bizjak,
Frederick F Razzaghi,
Frederick M Lochner,
Gilbert J Heidenblut,
Hugh M Mcclure, II,
Jeffrey A Sincek,
Jonathan W Chapman,
Joshua P Wireman,
Joshua S Hunt,
Karen M Kondas,
Kelli L Wilkinson,
Kenneth E Felkley,
Lauren N Howard,
Lauren N Smith,
Laurissa S Flowers,
LCDR Anastasia M Piliafas Brown,
Lori S Lawless,
Marcellinus D Dordunoo,
Mark E Parmon,
Matthew B Casale,
Matthew H Pitts,
Melissa J Garcia,
Merideth K Rose,
Michael P Sheehan,
Michael S Araneta,
Monica M Mcclure,
Nerizza B Guerin,
Nicholas L Paulin,
Patricia A Morrow,
Phillip M Pontikos,
Rachel C Harrington,
Rebecca Rodriguez,
Rosanna M Goodrich,
Rosanna M Vaccaro,
Sandra A Hughes,
Sean R Marcsisin,
Sharon K Thoma, PharmD,
Shirshendu K Deb, PhD,
Shusheen A Alexander,
Steven B Hertz,
Steven P Donald,
Suzanne M Healy,
Suzanne M Muchene,
Tajah L Blackburn,
Ted L Anderson,
Tyra S Wisecup,
Ucheabuchi Cchudi Nwankwor,
William J Leonard,
Zachary A Bogorad,
Zhigang Sun, PhD
Vipulchandra N Dholakia's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2016 | FDA 483 | Glaropharm AG - Form 483, 2016-03-04 |
May, 2013 | EIR | West-Ward Columbus Inc. - EIR, 2013-05-24 |
July, 2010 | FDA 483 | Nostrum Laboratories, Inc. - Form 483, 2010-07-16 |
March, 2015 | FDA 483 | Bell-More Labs Inc - Form 483, 2015-03-13 |
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