# FDA Inspection 1090483 - Liveyon - May 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/liveyon/6a4f3711-2f4e-42c0-a52b-8c7be1471730
Source feed: FDA_Inspections

> FDA Inspection 1090483 for Liveyon on May 23, 2019. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1090483
- Company Name: Liveyon
- Inspection Date: 2019-05-23
- Classification: Official Action Indicated (OAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1090483 - 2019-05-23](https://www.keypedia.com/records/fda_inspections/liveyon/35028515-9b44-4834-a285-698b079a9e7a)
- [FDA Inspection 1066677 - 2018-09-21](https://www.keypedia.com/records/fda_inspections/liveyon/2e433b88-3234-427e-a557-e9117bb32ec6)
- [FDA Inspection 1066677 - 2018-09-21](https://www.keypedia.com/records/fda_inspections/liveyon/ab1300f7-96f6-41c4-b36b-a28453d418a4)

Company: https://www.keypedia.com/companies/liveyon/668e46df-24a9-4a18-baf6-9d0752315ec0

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