# FDA Inspection 1067753 - KEDPLASMA LLC - September 20, 2018

Source: https://www.keypedia.com/records/fda_inspections/kedplasma-llc/742a552d-73b5-42d2-b23c-40d1a6046f41
Source feed: FDA_Inspections

> FDA Inspection 1067753 for KEDPLASMA LLC on September 20, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1067753
- Company Name: KEDPLASMA LLC
- Inspection Date: 2018-09-20
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

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- [FDA Inspection 756105 - 2011-12-01](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/ed561e3f-8c54-482a-9b23-02741f0d9259)

Company: https://www.keypedia.com/companies/kedplasma-llc/030db0bf-c975-4cae-ba37-f4e7507620db

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