FDA Investigator Laura A Grumenfelder
Laura A Grumenfelder has conducted inspections on 17 sites in 1 countries as of 08 Aug 2023. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
17
Last Inspection Date:
08 Aug 2023
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 Laura A Grumenfelder:
Aaron J Poloni,
Alex T Goodman,
Amy R Glynn,
Aric M Sonnenschein,
Arturo De La Garza,
Avery B Cromwell,
Brent W Higgs,
Brian M Campbell,
Brittany R Laymon,
Carl A Huffman, III,
Carrie L Doupnik,
Chase S Baldwin,
Daniel J Gorski,
David Castillo,
Debra D Devlieger,
Edwardstine J Reese,
Elizabeth L Holmes,
Elvin R Smith,
Erin L Nagel,
Erin M Holliman,
Estefania F Garber,
Ginger M Sykes,
Holly L Miller,
Ifueko Osemwota,
James R Montero,
Jennifer A D'angelo,
Joseph M Willems,
Kacie M Crowther,
Kamara Co,
Kate L Allen,
Kayla D Smith,
Kevin T Gerrity,
LT Mark A Chen, MPH,
Margaret N Klug,
Margaret N Persich,
Mark G Peterson,
Matthew J Hansen,
Matthew R Buenconsejo,
Megan T Wright,
Michael E Barta,
Miguel Gmanzano Maldonado,
Nathan R Moon,
Neil J Traaen,
Paula P Demichael,
Rebecca S Secrist,
Rodrigo O Chipres,
Roger J Adams,
Shane E Rainey,
Sullan,
Suyang Qin,
Tracy K Li,
Wayne W Grundstrom,
Wendy A Johnecheck
Laura A Grumenfelder's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2017 | FDA 483 | CONAGRA BRANDS CORPORATION - Form 483, 2017-07-13 |
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