# FDA Inspection 1210801 - KEDPLASMA LLC - May 24, 2023

Source: https://www.keypedia.com/records/fda_inspections/kedplasma-llc/9acdd033-e8ae-4823-8eba-c7244b188d1a
Source feed: FDA_Inspections

> FDA Inspection 1210801 for KEDPLASMA LLC on May 24, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210801
- Company Name: KEDPLASMA LLC
- Inspection Date: 2023-05-24
- 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 1210801 - 2023-05-24](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/baed4173-c162-410b-b5a6-d122e02fd495)

Company: https://www.keypedia.com/companies/kedplasma-llc/03d7be01-b16e-4c3b-8986-6ce4e5bb5dad

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