# Vitalant – FDA Inspection, Sep 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/vitalant/e5ccbc36-9dd3-44a6-bdb6-c439a6be404d
Source feed: FDA_Inspections

> FDA inspection 848922 of Vitalant, September 18, 2013. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 848922
- Company Name: Vitalant
- Inspection Date: 2013-09-18
- 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 1115247 - 2019-11-05
- FDA Inspection 1049590 - 2018-04-06
- FDA Inspection 986765 - 2016-09-14
- FDA Inspection 743495 - 2011-08-26

Company: https://www.keypedia.com/companies/vitalant/2f2a5f9b-61b0-4e3b-8295-ebc9f010abc8

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