# FDA Inspection 1108221 - FMI LLC - October 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/fmi-llc/e0cb64d1-2b25-4fba-b815-3ac580e05558
Source feed: FDA_Inspections

> FDA Inspection 1108221 for FMI LLC on October 24, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1108221
- Company Name: FMI LLC
- Inspection Date: 2019-10-24
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1221750 - 2023-10-23](https://www.keypedia.com/records/fda_inspections/fmi-llc/f39c64c6-c66e-4e53-a848-c5f3c8fcfec8)
- [FDA Inspection 1221750 - 2023-10-23](https://www.keypedia.com/records/fda_inspections/fmi-llc/391d274f-c38c-4f07-a42f-53747a756b1c)
- [FDA Inspection 1108221 - 2019-10-24](https://www.keypedia.com/records/fda_inspections/fmi-llc/c95c2cbb-db46-4268-a303-a2010ddea75b)

Company: https://www.keypedia.com/companies/fmi-llc/eec78946-5337-4998-9291-9194f6b4f08e

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