# FDA Inspection 1197483 - ORPHEUS MEDICAL USA INC - February 02, 2023

Source: https://www.keypedia.com/records/fda_inspections/orpheus-medical-usa-inc/0d70f5e2-9e2f-4fa2-a811-a607f44fa74b
Source feed: FDA_Inspections

> FDA Inspection 1197483 for ORPHEUS MEDICAL USA INC on February 02, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1197483
- Company Name: ORPHEUS MEDICAL USA INC
- Inspection Date: 2023-02-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1141348 - 2019-02-06](https://www.keypedia.com/records/fda_inspections/orpheus-medical-usa-inc/92d068eb-04f1-4041-9360-ea53151dc9a7)
- [FDA Inspection 1141348 - 2019-02-06](https://www.keypedia.com/records/fda_inspections/orpheus-medical-usa-inc/5619a19e-bb31-488b-bb91-a2fcd4a55ae2)

Company: https://www.keypedia.com/companies/orpheus-medical-usa-inc/da401f56-3b58-45ae-8edf-e2a83230bf5c

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