FDA Inspection
KedPlasma LLCKedPlasma LLC – FDA Inspection, Mar 21, 2019
Record Details
This FDA Inspection record concerns KedPlasma LLC, with an inspection on March 21, 2019, issued by the Atlanta District Office, covering biologics.
- Office
- Atlanta District Office
- People
- Christopher M. Cox
- Cordelia J. Brammer (Company Rep)
- Judy E. Ciaraldi (Issuing Officer)
View Company Profile
ID · 537dec29-6b9b-4eed-9d00-36531e47a04f
Inspection Facts
- Inspection number
- 1091597
- FDA center
- Biologics
- Outcome
- Form 483 issued
Other FDA inspections of KedPlasma LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 21, 2026 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| January 8, 2026 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| December 5, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 9, 2025 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 24, 2023 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for KedPlasma LLC
- FDA Inspection 1314436 - 2026-04-21
- FDA Inspection 1298204 - 2026-01-08
- FDA Inspection 1294768 - 2025-12-05
- FDA Inspection 1285778 - 2025-10-09
- FDA Inspection 1219073 - 2023-07-24
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.