# FDA Inspection 1205390 - KEDPLASMA LLC - April 06, 2023

Source: https://www.keypedia.com/records/fda_inspections/kedplasma-llc/542b2457-17a1-486a-9fb2-8dc1a729929d
Source feed: FDA_Inspections

> FDA Inspection 1205390 for KEDPLASMA LLC on April 06, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205390
- Company Name: KEDPLASMA LLC
- Inspection Date: 2023-04-06
- 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 1305614 - 2026-01-16](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/965d7fe7-7843-46d5-8fb5-935bbd0431b9)
- [FDA Inspection 1205390 - 2023-04-06](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/1f5c31a4-9207-4b56-9063-1b8e39786b69)

Company: https://www.keypedia.com/companies/kedplasma-llc/bc105dd3-9568-40c0-b593-dd0dccab49ad

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