# FDA Inspection 1081930 - KEDPlasma LLC - February 27, 2019

Source: https://www.keypedia.com/records/fda_inspections/kedplasma-llc/c63fa742-408a-455e-b256-f52946ef7ad5
Source feed: FDA_Inspections

> FDA Inspection 1081930 for KEDPlasma LLC on February 27, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1081930
- Company Name: KEDPlasma LLC
- Inspection Date: 2019-02-27
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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Company: https://www.keypedia.com/companies/kedplasma-llc/95a63459-05bc-496a-a471-d5c45fe78da1

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