FDA Investigator Andrew F Saunders
Andrew F Saunders has conducted inspections on 2 sites in 1 countries as of 06 Apr 2015. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
2
Last Inspection Date:
06 Apr 2015
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 Andrew F Saunders:
Andrew Saunders,
Anthony D Peterson,
Cheryl G Scott,
David J Leray,
David R Heiar,
Fatimah Omar,
Jessica A Stephens,
Justin N Henson,
Leslie R Morgan,
Lezette M Earhart,
Lindsay H Bertling,
Lindsay M Hughes,
Marcus L Head,
Maressa L Mills,
Markeesa M Scales,
Miguel J Merriweather,
Patrick C Dooley,
Peggy A Stogner,
Priya J Rathnam,
Robert E Hultman,
Sandy L Atkins,
Shirhonda D Thorn,
Thomas B Smith,
Thomas O Morgan,
Wilvor K Butler
Andrew F Saunders's Documents
Publish Date | Document Type | Title |
---|---|---|
December, 2009 | FDA 483 | Unilever Covington - Form 483, 2009-12-11 |
April, 2015 | FDA 483 | Blue Bell Creameries Inc L.P - Form 483, 2015-04-30 |
April, 2015 | FDA 483 Response | Blue Bell Creameries Inc L.P - Form 483R, 2015-05-22 |
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