# FDA Inspection 1097452 - Vitalant - July 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/vitalant/26cc3371-aac5-4e23-8fc4-15a8ef5110b3
Source feed: FDA_Inspections

> FDA Inspection 1097452 for Vitalant on July 24, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097452
- Company Name: Vitalant
- Inspection Date: 2019-07-24
- 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 917998 - 2015-02-06](https://www.keypedia.com/records/fda_inspections/vitalant/62a706e3-8d99-4a89-b399-e7aa22ea6661)

Company: https://www.keypedia.com/companies/vitalant/22d14b59-7237-4669-8216-ec5ca5dd7434

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