# FDA Inspection 1029792 - Vitalant - October 03, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitalant/7cfe2497-017b-412b-9068-b0588042543d
Source feed: FDA_Inspections

> FDA Inspection 1029792 for Vitalant on October 03, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029792
- Company Name: Vitalant
- Inspection Date: 2017-10-03
- 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 1159683 - 2021-12-17](https://www.keypedia.com/records/fda_inspections/vitalant/087cd7da-a4c5-420b-9f85-e06df78ebec6)

Company: https://www.keypedia.com/companies/vitalant/45cab940-cb7c-41c3-bda5-aa5ae43b1fe8

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