# FDA Inspection 900620 - Vitalant - October 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/vitalant/a3f2c2ba-5bf6-4b63-a2f9-ec756778fbab
Source feed: FDA_Inspections

> FDA Inspection 900620 for Vitalant on October 22, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 900620
- Company Name: Vitalant
- Inspection Date: 2014-10-22
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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Company: https://www.keypedia.com/companies/vitalant/61f12655-5b50-45b8-a879-d8a4b1c058e6

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