FDA Investigator John J Welsh, PhD

John J Welsh, PhD has conducted inspections on 3 sites in 1 countries as of 19 May 2008. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
3
Last Inspection Date:
19 May 2008
Investigator Role:
FDA Investigation Participant
Redica ID:
100008526
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with John J Welsh, PhD:
Ana P Barido, Barbara J Holladay, Brian R Cronenwett, Carla C Tuite, Carmen Y Fisher, Carol Rivera Lopez, PhD, Catherine Whiteside, PhD, Charles M Kerns, BLT DO, Christine M Whitby, CSO, Cynthia A Harris, MD, RN, David K Glasgow, Diana M Guidry, Dr. Abhijit Raha, PhD, Emest F Bizjak, George Ivan Wey, Hector Jcolon Torres, Jacqueline A O'shaughnessy, PhD, Jeffery A Hangartner, Jin Young Park, PhD, John A Iwen, John Kadavil, PhD, Kara L Roden, Karen M Montgomery (KMM), Kenneth Nieves, Kevin A Beavers, Kristi M Hampton Thurston, LCDR Audra J Lenhart, LT Melanie M Mayor, USPHS, Lynette P Salisbury, Melissa J Garcia, Michael F Skelly, PhD, Sherry L Secrist, BLT DO, Steven J Thurber, Tamika E Allen, RN, Ted L Anderson, Tracy L Taras, PhD, William F Lagud, Jr

John J Welsh, PhD's Documents

Publish Date Document Type Title
May, 2008 FDA 483 Response Covance Laboratories, Inc. - Form 483R, 2008-06-25
February, 2000 EIR Bio-Kinetic Clinical Applications, LLC - EIR, 2000-02-03
June, 2002 EIR Covance Laboratories, Inc. - EIR, 2002-06-21
June, 2002 FDA 483 Response Covance Laboratories, Inc. - Form 483R, 2002-06-21
June, 2002 FDA 483 Covance Laboratories, Inc. - Form 483, 2002-06-21
May, 2008 EIR Covance Laboratories, Inc. - EIR, 2008-05-22

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