# FDA Inspection 1024859 - Vitalant - August 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitalant/4a346cad-3194-4cbb-805b-efb2bedaa77a
Source feed: FDA_Inspections

> FDA Inspection 1024859 for Vitalant on August 16, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024859
- Company Name: Vitalant
- Inspection Date: 2017-08-16
- 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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Company: https://www.keypedia.com/companies/vitalant/b86a560a-90c0-4c98-b94e-a8bd54611bee

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