FDA Investigator Zonglin Hu
Zonglin Hu has conducted inspections on 4 sites in 2 countries as of 22 Aug 2022. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
4
Last Inspection Date:
22 Aug 2022
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Germany
FDA Investigators that have inspected at least one site in common with Zonglin Hu:
Ashley N Queen, PhD,
Bo Chi, PhD,
Cynthia Jim, CSO,
Daniel J Lahar,
David P Vanhouten,
Erika V Butler,
Jacqueline Mdiaz Albertini,
James L Dunnie, Jr,
Joey V Quitania,
Jonathan B Lewis,
José E Meléndez,
Justin A Boyd,
Kathy E Noe,
Laurie B Frazier,
Lorie S Hannappel,
Michael E Maselli,
Michael R Klapal,
Michael Shanks, MS,
Mihaly S Ligmond,
Mizanne E Lewis,
Mra Mcculloughj,
Olumide A Martins,
Omotunde O Osunsanmi,
Philip H Lafleur,
Prabhu P Raju,
Rafael Padilla,
Ralph H Vocque,
Robert C Coleman,
Robert J Martin,
Rose Ashley,
Russell K Riley,
Santos E Camara,
Scott T Ballard,
Shannon A Gregory,
Sharon K Thoma, PharmD,
Sidney B Priesmeyer,
Simone E Pitts,
Stephanie A Slater, MS,
Stephen C Smith,
Steven C Madzo,
Susan P Bruederle,
Thomas J Arista,
Thomas W Nerney,
Thuy T Nguyen, LCDR,
Tonnie L Carter,
Wayne E Seifert
Zonglin Hu's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2022 | FDA 483 | Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) - Form 483, 2022-08-26 |
July, 2017 | EIR | Biotechne, Inc. - EIR, 2017-07-20 |
August, 2022 | FDA 483 | Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Schuetzenstrasse) - Form 483, 2022-08-19 |
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