FDA Investigator Shaun M Stracener

Shaun M Stracener has conducted inspections on 72 sites in 1 countries as of 08 Jun 2022. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
72
Last Inspection Date:
08 Jun 2022
Investigator Role:
FDA Investigator
Redica ID:
100008129
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Shaun M Stracener:
Alicia M Frees, Alysia C Alger, Aqualia L Nelson, Ashlee M Ward, Avery J Dennis, Bonnie E Pierson, Brandi E Williams, Brittany D Terhar, Bruce E Taylor, Chad W Rice, Christopher D Snyder, Cody J Alley, Collins M Mason, Cynthia M Goudeau, Dana D Carter, SR DDS, Darrah, Diana K Krepel, Dwight D Ferguson, Elizabeth P Mayer, Eric C Fox, Eric C Nielsen, Eric M Mueller, PharmD, Erin C Dugan, Heath W Cartwright, Hiwot A Kesi, Huffmanc, Ingrid Y Johnson, Janesa A Licorish, Janete A Eaker, Janete A Oliveira, Jeffrey B Moody, Jessica E Hensley, Jessica L Peterson, Jim Griess, Johnson, Jonathan R Campos, Joselin P Baray Alvarado, Joseph R Lambert, Kamara Mo, Katherine M Taylor, Kathleen J Close, Kevin A Beavers, Kristi B Panzer, LCDR Ismael Olvera, IV, Linda K Cline, Linhart, Lionell L Thomas, Lisa L Flores, Lori A Gioia, Louis S Chen, Lyndsey G Smith, Marion D Wimberly, Jr, Mathur, Meisha Waters, Melissa N Simanton, Melissa N Wilson, Melva Ball, Michael A Feingold, Michelle C Webb, Minerva Rogers, Ngoc B Kelsch, Nia K Walker, Peter E Gruman, Rashonda N Rucker, Raymond T Anderson, Rita K Kabaso, Robin E Hayes, Rodney D Combs, Ron R Pearson, Shaun M Olson, Sondra L Phillips, Steven C Clifford, Steven P Allen, Stroman, Tara M Aikens, Tara M Humfeld, Teresa S Johnson, Timothy D Evans, Tristian E Strait, Walsworth, Zachary A Bogorad

Shaun M Stracener's Documents

Publish Date Document Type Title
July, 2018 FDA 483 Oakmont Products, LLC - Form 483, 2018-07-13
June, 2022 FDA 483 ByHeart Inc dba Blendhouse Allerton - Form 483, 2022-06-30
July, 2018 FDA 483 IRCA Group USA LLC - Form 483, 2018-07-25

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