FDA Investigator Carla C Cummins
Carla C Cummins has conducted inspections on 8 sites in 1 countries as of 21 Dec 2023. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
8
Last Inspection Date:
21 Dec 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 Carla C Cummins:
Alan R Condon,
Althea A Williams,
Amy C Jordan,
Barbara G Swan,
Brenda P King,
Carla C Tuite,
Carlos Chavez,
Darin S Wiegers,
Dolores Harper,
Donna J Clevenger,
Dr. Sriram Subramaniam, PhD,
Edmund F Mrak, Jr,
Elizabeth B Griffin,
Gary J Hagan,
George T Allen, Jr,
James H Tanner,
James P Finn,
John A Sciacchitano,
John P Mistler,
Jonathan G Matrisciano,
Justine M Corson,
Karen Mcnabb Noon,
Katherine D Adams,
Lauren M Lawrance,
Laurie B Frazier,
LCDR Debra Emerson,
Leo B Zadecky,
Lori M Newman,
Matthew C Watson,
Maura Rooney,
Meredith L Miller,
Michael J Casey,
Philip Kreiter,
Richard B Mcaroy,
Richard H Penta,
Robert J Martin,
Rory K Geyer,
Sandra P White,
Seth A Mailhot,
Stacey S Degarmo,
Stephen C King,
Suzanne M Healy,
Terry C Kimball
Carla C Cummins's Documents
Publish Date | Document Type | Title |
---|---|---|
April, 2006 | FDA 483 | Polycarbon Industries, Inc. - Form 483, 2006-04-19 |
December, 2004 | FDA 483 | Haemonetics Corporation - Form 483, 2004-12-20 |
May, 2003 | FDA 483 | Tomy International Inc. - Form 483, 2003-05-09 |
June, 2003 | FDA 483 | Lantheus Medical Imaging, Inc. - Form 483, 2003-06-24 |
April, 2005 | FDA 483 | Boston Scientific Corporation - Form 483, 2005-04-07 |
May, 2005 | FDA 483 | Boston Scientific Corporation - Form 483, 2005-05-20 |
December, 2002 | FDA 483 | Parlex Polymer Flexible Circuits, Inc. - Form 483, 2002-12-13 |
February, 2006 | FDA 483 | Allen Medical Systems, Inc. - Form 483, 2006-02-01 |
June, 2003 | EIR | Lantheus Medical Imaging, Inc. - EIR, 2003-06-24 |
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