FDA Investigator Carol S Sanchez
Carol S Sanchez has conducted inspections on 9 sites in 3 countries as of 06 Jan 2005. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
9
Last Inspection Date:
06 Jan 2005
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Canada,
Mexico
FDA Investigators that have inspected at least one site in common with Carol S Sanchez:
Abby M Miller,
Alexandra B Pitkin,
Allen F Hall,
Ana M Pietsch,
Barbara Janine Breithaupt,
Bonnie I Needleman,
Brian Ravitch,
Bush,
Cathleen A Carr Sharpe,
Dana M Klimavicz,
David G Whitman,
David Hernandez,
David Y Hernandez,
Davis,
Debra D Devlieger,
Dr. Sriram Subramaniam, PhD,
Erica Aspinwall Brown,
Francisco,
Garciam,
Geoffrey M Leist,
Glorioso M Pama,
Gulshan R Anand,
Henry E Carrillo,
Iris C Macinnes,
Jacqueline A O'shaughnessy, PhD,
John R Myung,
Judy C Nepsa,
Kelvin X Sanders,
Kevin T Gerrity,
Lisa P Oakes,
Martin K Yau, PhD,
Maurice M Sheehan,
Maximiano Perez,
Michael D Garcia,
Michael F Skelly, PhD,
Natalie J Ayoub,
Natalie J Reese,
Naveen B Walker,
Nilufer M Tampal, PhD,
Patti A Walters,
Raphelia Spisso,
Rebecca I Campalans,
Rochelle A Rolnik,
Rocio Guzman Velazquez,
Romero,
Ruth P Dixon,
Sara Jdent Acosta,
Sarah A Hassas,
Scott B Laufenberg,
Sonia R Peterson,
Sparky L Bartee,
Sundy V Sedwick,
Susan F Laska, MS,
Tawny L Colling,
Thanh M Andrews,
Thao T Kwan,
Ve T Vuong
Carol S Sanchez's Documents
Publish Date | Document Type | Title |
---|---|---|
January, 2005 | EIR | Catalina Offshore Products, Inc - EIR, 2005-01-12 |
March, 2001 | EIR | SPR De RI Legumbrera San Luis - EIR, 2001-03-19 |
July, 2003 | FDA 483 Response | MDS Pharma Services - Form 483R, 2003-07-17 |
July, 2003 | FDA 483 | MDS Pharma Services - Form 483, 2003-07-17 |
July, 2003 | EIR | MDS Pharma Services - EIR, 2003-09-24 |
August, 2000 | EIR | Pepsi Bottling Group - EIR, 2000-08-15 |
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