# FDA Inspection 1180601 - Vitalant - August 30, 2022

Source: https://www.keypedia.com/records/fda_inspections/vitalant/8783ca0d-8615-4ffd-8ae6-52b373bde003
Source feed: FDA_Inspections

> FDA Inspection 1180601 for Vitalant on August 30, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180601
- Company Name: Vitalant
- Inspection Date: 2022-08-30
- Classification: No Action Indicated (NAI)
- Project Area: Vaccines and Allergenic Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1180601 - 2022-08-30](https://www.keypedia.com/records/fda_inspections/vitalant/1f40d34e-02f7-47ee-90fa-50ceb6952138)

Company: https://www.keypedia.com/companies/vitalant/a1f49468-615c-4adf-b10d-151bd303090b

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