# FDA Inspection 1084688 - Imbio LLC - March 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/imbio-llc/c1cfbc25-9f4d-44a1-bf5f-8bf723e2ed07
Source feed: FDA_Inspections

> FDA Inspection 1084688 for Imbio LLC on March 21, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1084688
- Company Name: Imbio LLC
- Inspection Date: 2019-03-21
- 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 1084688 - 2019-03-21](https://www.keypedia.com/records/fda_inspections/imbio-llc/c92326b1-7017-45f5-bed0-2f7f81bd3f22)
- [FDA Inspection 952973 - 2015-12-15](https://www.keypedia.com/records/fda_inspections/imbio-llc/fe8165f5-1c31-4ef9-95c9-ae5219c7feb6)

Company: https://www.keypedia.com/companies/imbio-llc/76753201-97e2-409d-a595-0e1259e05bdd

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