# Vitalant – FDA Inspection, Dec 9, 2013

Source: https://www.keypedia.com/records/fda_inspections/vitalant/25f79a2d-224f-4b73-92b7-6586f5b44734
Source feed: FDA_Inspections

> FDA inspection 858500 of Vitalant, December 09, 2013. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 858500
- Company Name: Vitalant
- Inspection Date: 2013-12-09
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1256872 - 2024-12-05
- FDA Inspection 1180193 - 2022-09-14
- FDA Inspection 1033943 - 2017-11-28
- FDA Inspection 958203 - 2016-01-25
- FDA Inspection 783582 - 2012-05-22

Company: https://www.keypedia.com/companies/vitalant/96cef0a4-a35a-4fdf-aec9-4a7559868eb0

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