# FDA Inspection 1090414 - Lumibird Medical Inc - May 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/lumibird-medical-inc/164d5bf0-dd86-43fd-bb46-8ee851a9b5c5
Source feed: FDA_Inspections

> FDA Inspection 1090414 for Lumibird Medical Inc on May 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1090414
- Company Name: Lumibird Medical Inc
- Inspection Date: 2019-05-07
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1004044 - 2017-01-18](https://www.keypedia.com/records/fda_inspections/lumibird-medical-inc/6f187da6-cb30-4c6a-b5be-97c8b336e909)
- [FDA Inspection 962771 - 2016-03-16](https://www.keypedia.com/records/fda_inspections/lumibird-medical-inc/6c215986-e806-4065-891e-3145b23a8cc9)

Company: https://www.keypedia.com/companies/lumibird-medical-inc/8f007a0c-d355-4a17-b3d0-90ad3d8326bf

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