# FDA Inspection 1086552 - Medibio USA LLC - April 16, 2019

Source: https://www.keypedia.com/records/fda_inspections/medibio-usa-llc/13fa5c4b-e5de-4971-ae09-dcc205457274
Source feed: FDA_Inspections

> FDA Inspection 1086552 for Medibio USA LLC on April 16, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1086552
- Company Name: Medibio USA LLC
- Inspection Date: 2019-04-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1086552 - 2019-04-16](https://www.keypedia.com/records/fda_inspections/medibio-usa-llc/c7259c1c-008f-4543-9185-a64cb5b6831e)

Company: https://www.keypedia.com/companies/medibio-usa-llc/2930cb4b-ff46-4338-83fd-708c8dca7336

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
