# FDA Inspection 786172 - Vitalant - June 13, 2012

Source: https://www.keypedia.com/records/fda_inspections/vitalant/9b15be3b-c8ea-4cd2-a84d-96ab4f365edf
Source feed: FDA_Inspections

> FDA Inspection 786172 for Vitalant on June 13, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 786172
- Company Name: Vitalant
- Inspection Date: 2012-06-13
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1229052 - 2024-01-31](https://www.keypedia.com/records/fda_inspections/vitalant/9b899e95-1b63-449d-864c-c6a76c02ef2e)
- [FDA Inspection 1084078 - 2019-03-08](https://www.keypedia.com/records/fda_inspections/vitalant/78b716b6-61cd-42a3-8f0e-2781b021916c)
- [FDA Inspection 981014 - 2016-06-30](https://www.keypedia.com/records/fda_inspections/vitalant/ba386d56-9951-4a66-a829-d03d23d1eb2e)
- [FDA Inspection 948428 - 2015-10-14](https://www.keypedia.com/records/fda_inspections/vitalant/4f93d166-18d0-4de2-b9f4-1a99edbf1a5f)
- [FDA Inspection 910467 - 2015-01-30](https://www.keypedia.com/records/fda_inspections/vitalant/54d7a144-9639-4b34-b00e-c38e07659556)

Company: https://www.keypedia.com/companies/vitalant/4650dc53-3a85-428f-832d-2d3e73fc96aa

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