# FDA Inspection 1176361 - SOPRO - July 21, 2022

Source: https://www.keypedia.com/records/fda_inspections/sopro/b9b423d8-f9fb-4551-9809-2e249495cd47
Source feed: FDA_Inspections

> FDA Inspection 1176361 for SOPRO on July 21, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1176361
- Company Name: SOPRO
- Inspection Date: 2022-07-21
- 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 1176361 - 2022-07-21](https://www.keypedia.com/records/fda_inspections/sopro/c569c5a1-9cd7-4a06-8658-232ab823bd4b)

Company: https://www.keypedia.com/companies/sopro/329d6199-0326-4db0-8eb0-86c71d454448

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