# FDA Inspection 1024632 - Vitalant (Harmar - Fox Chapel Area) - August 22, 2017

Source: https://www.keypedia.com/records/fda_inspections/vitalant-harmar-fox-chapel-area/3e164254-3587-4fa5-ae7b-98d0fe936111
Source feed: FDA_Inspections

> FDA Inspection 1024632 for Vitalant (Harmar - Fox Chapel Area) on August 22, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024632
- Company Name: Vitalant (Harmar - Fox Chapel Area)
- Inspection Date: 2017-08-22
- 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-harmar-fox-chapel-area/4f35bb4a-b596-4983-a8b9-eec0cd1f21bc

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