# Vitalant – FDA Inspection, Nov 20, 2008

Source: https://www.keypedia.com/records/fda_inspections/vitalant/e98e0eec-67a8-42df-8f0c-342cc56d556f
Source feed: FDA_Inspections

> FDA inspection 548022 of Vitalant, November 20, 2008. Classification: No Action Indicated (NAI). 7 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 548022
- Company Name: Vitalant
- Inspection Date: 2008-11-20
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- 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 1305000 - 2026-02-12
- FDA Inspection 1162743 - 2022-02-09
- FDA Inspection 1074889 - 2018-12-04
- FDA Inspection 988926 - 2016-10-18
- FDA Inspection 900581 - 2014-10-22

Company: https://www.keypedia.com/companies/vitalant/6556e70e-5519-45d8-96e5-dd55f22ef944

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