# Vitalant – FDA Inspection, Jan 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/vitalant/66d9ecd1-0128-4784-8b2f-d185bb09b6b0
Source feed: FDA_Inspections

> FDA inspection 818297 of Vitalant, January 30, 2013. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 818297
- Company Name: Vitalant
- Inspection Date: 2013-01-30
- 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 1221124 - 2023-10-24
- FDA Inspection 1076516 - 2018-12-19
- FDA Inspection 1028490 - 2017-08-25
- FDA Inspection 927824 - 2015-04-30
- [FDA Inspection 746605 - 2011-09-20](https://www.keypedia.com/records/fda_inspections/vitalant/d51f7f24-e882-42e6-af52-4a36250ddd6f)

Company: https://www.keypedia.com/companies/vitalant/641596d7-7712-4f90-86e8-c1b6b93683dc

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