FDA Investigator Sarah M Parkinson
Sarah M Parkinson has conducted inspections on 42 sites in 2 countries as of 15 May 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
42
Last Inspection Date:
15 May 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Greece
FDA Investigators that have inspected at least one site in common with Sarah M Parkinson:
Abby Lmozeke Baker,
Alissa C Rice,
Amanda M Osteen,
Andre L Duhon,
Andrew M Kupper,
Andrew Saunders,
Anetra E Wyatt,
Ashley D Abraham,
Ashley N Jeans,
Brandon C Heitmeier,
Caitlin L Almonrode,
Carl A Huffman, III,
Casey L Hamblin,
Charvais S Hill,
Cherie T Parker,
Cheryl G Scott,
Cheryl L Watson,
Christian L Witkovskie,
Clendening,
Clifton C Francis,
Craig P Seaborn,
Cynthia L Medlin,
Danielle M Maddox,
David R Heiar,
Debra A Taylor,
Decima L Thompson,
Decima L Washington,
Dyanthony T Jenkins,
Herbert M Corbello,
Herman S Clincy,
Hugh A Grimoldby,
Ivy E Sweeney,
Javonica F Penn,
Jessica M Wooten,
John E Russell, Jr,
Johnathan M Crayton,
Jon C Hackleman,
Josiah D Davis,
Justin N Henson,
Karen M Cooper,
Kari L Batey,
Kathryn Suttling,
Kerry Ann Latham,
Kimberly A Dutzek,
Kimberly L Mcmillan,
Krista T Ferry,
Krista W Whitten,
Laura L Staples,
Linda A Gregory Duty,
Lindsay H Bertling,
Lindsay M Hughes,
Llopis,
Luckner Jean Marie,
Maressa L Mills,
Margaret E Slimbach,
Marissa R Stough,
Mark A Darnell,
Markeesa M Scales,
Marshall H Kinsey,
Mary B Sheets,
Melanie L Drayton,
Nadia V Simmons,
Nicole D Lyons,
Peggy A Stogner,
Robert E Hultman,
S Lori Brown, PhD MPH,
Sandricka M Mosley,
Sandy L Atkins,
Sarah Parkinson,
Scott A Watson,
Scott W Fox,
Shalonda L Gatewood,
Shannon Atlas,
Shelton L Stribling,
Shondra N Gipson,
Stephen G Mclane,
Steven D Dittert,
Talmane J Fisher,
Thomas B Smith,
Thomas C Mclean, CFS,
Travis E Chapman,
Wayne S Fortenberry,
Whitney M White,
Zachary J Conlin,
Zada L Giles
Sarah M Parkinson's Documents
Publish Date | Document Type | Title |
---|---|---|
October, 2022 | EIR | Taylor Farms Tennessee, Inc. - EIR, 2022-10-28 |
October, 2023 | FDA 483 | American Cruise Lines Inc. dba American Splendor - Form 483, 2023-10-17 |
February, 2024 | FDA 483 | Warner Herb Co. - Form 483, 2024-02-27 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
![FDA Investigator Profile Icon](/images/InspectorProfile.png)
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more