# FDA Inspection 1216476 - Genvion Corporation - July 28, 2023

Source: https://www.keypedia.com/records/fda_inspections/genvion-corporation/23b52120-0b49-4f0b-93eb-308a5358d95d
Source feed: FDA_Inspections

> FDA Inspection 1216476 for Genvion Corporation on July 28, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216476
- Company Name: Genvion Corporation
- Inspection Date: 2023-07-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 985034 - 2016-06-17](https://www.keypedia.com/records/fda_inspections/genvion-corporation/a09be837-b79c-4a95-8b3c-24945748ebb0)

Company: https://www.keypedia.com/companies/genvion-corporation/a4655b0c-e1a8-4645-bd02-3bcb514a08ce

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c