# FDA Inspection 1022662 - Kedplasma LLC - July 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/kedplasma-llc/770c5d49-19b0-4b7c-a77e-78eee0d80355
Source feed: FDA_Inspections

> FDA Inspection 1022662 for Kedplasma LLC on July 28, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022662
- Company Name: Kedplasma LLC
- Inspection Date: 2017-07-28
- 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/3f3aacfd-d14e-4ef0-9b1e-fd0853808e6a

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