# FDA Inspection 998083 - Vitalant - December 06, 2016

Source: https://www.keypedia.com/records/fda_inspections/vitalant/45b8bd76-8a7b-4b2a-9497-4334f2fe6994
Source feed: FDA_Inspections

> FDA Inspection 998083 for Vitalant on December 06, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 998083
- Company Name: Vitalant
- Inspection Date: 2016-12-06
- 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 1238350 - 2024-04-25](https://www.keypedia.com/records/fda_inspections/vitalant/9874d6fd-f69e-47ea-a23f-484c3300a9dd)
- [FDA Inspection 1075128 - 2018-10-31](https://www.keypedia.com/records/fda_inspections/vitalant/8175f5d7-edc3-45da-bfca-192590e9b6a2)
- [FDA Inspection 913381 - 2015-02-06](https://www.keypedia.com/records/fda_inspections/vitalant/85cbb3de-a873-4476-9276-1a1af4c28c49)
- [FDA Inspection 856431 - 2013-10-30](https://www.keypedia.com/records/fda_inspections/vitalant/4162c0b2-c47a-43a0-b6a9-539b6eb16178)
- [FDA Inspection 752456 - 2011-11-01](https://www.keypedia.com/records/fda_inspections/vitalant/926404f5-bfbc-420d-b260-15f8abc351d8)

Company: https://www.keypedia.com/companies/vitalant/9255f2bb-a84f-4709-80e5-4bdc48212a2f

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