FDA Investigator Garrett W Steiner
Garrett W Steiner has inspections in 1 countries as of 27 Sep 2023. Garrett W Steiner has collaborated with a combined 1468 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
38
Last Inspection Date:
27 Sep 2023
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Alfred P Pistorio,
Alison A Nicoli,
Amos,
Amy L Mcintyre,
Anthony L Nicoli,
Anthony P Duran,
Billi Jom Johnson,
Bradley A Servais,
Bunce,
Carolyn A Warren,
Christina A Castineyra,
Christine M Erickson,
Como,
Courtney R Tiegs,
Dacia E Quick,
David B Wieneke,
Demetria L Lueneburg,
Dianna C Sonnenburg,
Duc Minh H Nguyen,
Edward A Fabiano,
Edward M James,
Elias H Wachter,
Elizabeth P Mayer,
Emily E Markgraf,
Fannie M Harrell,
Frank S Sedzielarz,
Franklin D Heisler,
Gina M Scholze,
Grant M Ruis,
Greg A Abel,
Howard A Burmester,
Jaclyn N Munsch,
Jake T Lane,
Jamie R Thompson,
Jane E Nelson,
Jasjeet K Sekhon,
Jean M Trimbo,
Jennifer R Mathern,
Jeremy L Tri,
Jonathan G Dillon,
Julie Woodberry,
Karen M Gasperic,
Karen M Jirele,
Karen M Labounty,
Karla J Youngberg,
Katherine A Clarke Girolamo,
Kenneth A Libertoski,
Kevin L Torgerson,
Kibily D Dembele,
Krista K Petersen,
Kristy E Zuroski,
Kyle J Mccracken,
Lauren E Sanger,
Linda V Weyer,
Mada A Tautges,
Margaret M Lubbers Solberg,
Maria E Treadwell,
Marissa S Steinhagen,
Mary M Finn,
Melissa D Kalik,
Melissa I Michurski,
Michael E Cimaglio,
Mohammed H Adam,
Paola E Lathrop,
Rebecca L Caulfield,
Rebecca L Keller,
Rebecca L Mullikin,
Rebecca L Zamora,
Robert H Claflin,
Robert J Waldorf,
Sana A Elassar,
Seth A Abbott,
State Agency,
Susan M Miller,
Terrance L Scheiber,
Theresa C Dziuk,
Theresa C Klaman,
Thomas S Donaldson,
Victoria L Palmer,
Wayne W Grundstrom,
Wendy L Trefethren Grang,
Zachary P Wachlarowicz
Garrett W Steiner's Documents
Publish Date | Document Type | Title |
---|---|---|
January, 2023 | FDA 483 | Mead Johnson and Co., LLC - Form 483, 2023-01-09 |
January, 2024 | FDA 483 | Mead Johnson and Co., LLC - Form 483, 2024-01-10 |
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](https://redica.com/document-store/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