# Vitalant – FDA Inspection, Jun 16, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitalant/e1e28767-7bdf-4f53-913e-abf8f40429cf
Source feed: FDA_Inspections

> FDA inspection 1017789 of Vitalant, June 16, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 7 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1017789
- Company Name: Vitalant
- Inspection Date: 2017-06-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1277087 - 2025-07-23
- FDA Inspection 1205605 - 2023-05-04
- FDA Inspection 1081616 - 2019-02-22
- FDA Inspection 936053 - 2015-07-23
- FDA Inspection 831898 - 2013-05-07

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/vitalant/d18d6603-e972-4b0a-82c0-9162571cfe46

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