# FDA Inspection 1196531 - Kedplasma LLC - January 26, 2023

Source: https://www.keypedia.com/records/fda_inspections/kedplasma-llc/cf630437-04ce-400b-b4a7-39f2a6182dd9
Source feed: FDA_Inspections

> FDA Inspection 1196531 for Kedplasma LLC on January 26, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1196531
- Company Name: Kedplasma LLC
- Inspection Date: 2023-01-26
- Classification: Voluntary Action Indicated (VAI)
- 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 1085589 - 2019-03-29](https://www.keypedia.com/records/fda_inspections/kedplasma-llc/46e91647-819b-4800-8bb6-23e074d7ec7e)
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Company: https://www.keypedia.com/companies/kedplasma-llc/3f3aacfd-d14e-4ef0-9b1e-fd0853808e6a

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