FDA Investigator Valerie Reed
Valerie Reed has conducted inspections on 3 sites in 1 countries as of 21 May 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
3
Last Inspection Date:
21 May 2024
Investigator Role:
FDA Investigation Participant
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Valerie Reed:
Alberto A Viciedo,
Allen Lou,
Amatul H Marium,
Anthony J Donato,
Barbara J Maulfair,
Christopher J Adams,
Dawn L Wydner,
Deborah B Nixon,
Denise M Visco, Investigator,
Dolores Harper,
Douglas C Kovacs,
Emily A Walters,
Emmanuel Jramos Maldonado,
Esteban Beltran,
Frank J Marciniak,
Guerlain Ulysse,
Helen B Ricalde,
Jean M Kelahan,
Jennifer A Bazergui,
Jennifer L Custodio,
Jennifer Macmillan,
Jonee J Mearns,
Karen E D'orazio,
Keith M Reilly,
Kelli F Dobilas,
Kerry A Kurdilla,
Kish Bolden,
Lata C Mathew, PhD,
Liatte Kreuger, PharmD,
Lisa Harlan,
Melba Trivera Clavell,
Michael Serrano,
Nerizza B Guerin,
Niketa Patel,
Paul L Bellamy,
Peter R Lenahan,
Richard D Manney,
Sandra Kershaw,
Sarah Forney,
Tara G Bizjak,
Tara R Gooen,
Valerie C Reed,
Victoria Spivak
Valerie Reed's Documents
Publish Date | Document Type | Title |
---|---|---|
February, 2005 | FDA 483 Response | SGS North America Inc. - Form 483R, 2005-03-03 |
November, 2003 | FDA 483 | Coutex, Inc. - Form 483, 2003-11-10 |
February, 2005 | FDA 483 | SGS North America Inc. - Form 483, 2005-02-07 |
March, 2002 | EIR | LifeCell Corporation - EIR, 2002-03-07 |
February, 2005 | EIR | SGS North America Inc. - EIR, 2005-02-07 |
November, 2003 | EIR | Coutex, Inc. - EIR, 2003-11-10 |
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