# FDA Inspection 1095941 - Modo, Inc. - June 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/modo-inc/332c2ac6-1196-4129-8bce-0d61092002ca
Source feed: FDA_Inspections

> FDA Inspection 1095941 for Modo, Inc. on June 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095941
- Company Name: Modo, Inc.
- Inspection Date: 2019-06-07
- 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 1095941 - 2019-06-07](https://www.keypedia.com/records/fda_inspections/modo-inc/83c9e983-5213-48ad-aa69-dac64a1cb362)

Company: https://www.keypedia.com/companies/modo-inc/b45d88a1-ab52-40e7-a1f4-7a4da605053d

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