FDA Investigator Amber M Capello Jones
Amber M Capello Jones has conducted inspections on 28 sites in 1 countries as of 17 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
28
Last Inspection Date:
17 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Amber M Capello Jones:
Aaron L Dunbar,
Allison M Scheck,
Althea A Williams,
Amy S Graf,
Benjamin E Bowen,
Benjamin J Smith,
Bernard P Heidt,
Brigitte K Hofmann,
Bryan J Love,
CDR Sean T Creighton,
Charles M Spyr,
Christina L Bigham,
Christine E Kelley,
Cynthia T Cain,
David J Gasparovich,
David P Moorhead,
Debara R Reese,
Donna F Campbell,
Elizabeth P Kinsella,
Genevieve E Ghand,
George G Calafactor,
Gina M Brackett,
Javonica F Penn,
Jeffrey A Sincek,
Jennifer L Gustavus,
Jennifer L Watson,
Joan A Loreng,
Joseph R Strelnik,
Katelyn Astaub Zamperini,
Kyle J Mccracken,
Lindsey M Schwierjohann,
Malik S Qaiser,
Maribeth G Grattan,
Maribeth G Niesen,
Marissa S Steinhagen,
Mark E Parmon,
Matt D Suedkamp,
Matthew H Pitts,
Patrick B Cummings,
Philip S Woodward,
Rosanna M Goodrich,
Rosanna M Vaccaro,
Roy C Stephens,
Shannon A Gregory,
Sharon L Matson,
Siobhan G Taylor,
Susan M Matthias,
Talmane J Fisher,
Tara C Singh,
Teresa K Kastner,
Tyler R Courtney,
William D Tingley
Amber M Capello Jones's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2023 | FDA 483 | Full Range Rehab LLC - Form 483, 2023-07-28 |
May, 2022 | FDA 483 | Surgical Appliance Industries Inc - Form 483, 2022-05-10 |
November, 2021 | FDA 483 | Elite Biomedical Solutions LLC - Form 483, 2021-11-09 |
July, 2021 | FDA 483 | CellEra LLC - Form 483, 2021-07-08 |
May, 2023 | FDA 483 | Mirac LLC - Form 483, 2023-05-11 |
April, 2022 | FDA 483 | CellEra LLC - Form 483, 2022-04-14 |
November, 2021 | FDA 483 | Baxter Healthcare Corporation - Form 483, 2021-11-19 |
September, 2021 | FDA 483 | Riverain Technologies Inc - Form 483, 2021-09-14 |
February, 2023 | FDA 483 | DimcoGray Inc. - Form 483, 2023-02-09 |
April, 2024 | FDA 483 | AeroBiotix LLC - Form 483, 2024-04-11 |
March, 2024 | FDA 483 | Electro Cap International Inc - Form 483, 2024-03-01 |
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