# FDA Inspection 1081610 - KEDPLASMA LLC - February 08, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/d0b27071-bf68-4d0d-a975-631ed65fab84
Source feed: FDA_Inspections

> FDA Inspection 1081610 for KEDPLASMA LLC on February 08, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1081610
- Company Name: KEDPLASMA LLC
- Inspection Date: 2019-02-08
- 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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- [FDA Inspection 967775 - 2015-11-20](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/78273276-2d48-496e-9e04-ade57639f746)
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Company: https://www.globalkeysolutions.net/companies/kedplasma-llc/f3f3364d-a117-4188-af10-a586451e385b

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