# FDA Inspection 1048417 - Relion Manufacturing Inc - February 13, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/relion-manufacturing-inc/154db504-4b44-4e7c-be36-02888d1dc6a4
Source feed: FDA_Inspections

> FDA Inspection 1048417 for Relion Manufacturing Inc on February 13, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048417
- Company Name: Relion Manufacturing Inc
- Inspection Date: 2018-02-13
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1048417 - 2018-02-13](https://www.globalkeysolutions.net/records/fda_inspections/relion-manufacturing-inc/0ddaa4eb-0b83-40d7-ac44-64f519ed5707)

Company: https://www.globalkeysolutions.net/companies/relion-manufacturing-inc/7c38652a-04f3-4a70-9182-def0813c873c

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