# FDA Inspection 1281658 - KEDPLASMA LLC - August 28, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/a8bf7690-fce1-43dd-a36c-2d84a44a8134
Source feed: FDA_Inspections

> FDA Inspection 1281658 for KEDPLASMA LLC on August 28, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1281658
- Company Name: KEDPLASMA LLC
- Inspection Date: 2025-08-28
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1281658 - 2025-08-28](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/89d94acb-6ebd-49c8-ae2c-d26c8ce61bf7)
- [FDA Inspection 1044857 - 2017-12-21](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/a0598540-ff8a-415f-8443-7e102eabfee2)

Company: https://www.globalkeysolutions.net/companies/kedplasma-llc/ed176bdf-a1cc-4d68-b57b-2356567cd37f

Office: https://www.globalkeysolutions.net/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d
