# FDA Inspection 1063846 - KEDPLASMA LLC - August 30, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/bc508a66-a380-4abf-994d-94db67367253
Source feed: FDA_Inspections

> FDA Inspection 1063846 for KEDPLASMA LLC on August 30, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063846
- Company Name: KEDPLASMA LLC
- Inspection Date: 2018-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 785202 - 2012-05-17](https://www.globalkeysolutions.net/records/fda_inspections/kedplasma-llc/7f57ad31-51a4-4684-84b5-63b037548ee4)

Company: https://www.globalkeysolutions.net/companies/kedplasma-llc/45d5360d-44eb-480a-81d5-3766043ff87d

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