# FDA Inspection 1054723 - Mobius Medical Systems, LP - June 07, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/mobius-medical-systems-lp/f8beab0f-eb5c-4396-929f-65f695eac33c/
Source feed: FDA_Inspections

> FDA Inspection 1054723 for Mobius Medical Systems, LP on June 07, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054723
- Company Name: Mobius Medical Systems, LP
- Inspection Date: 2018-06-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1054723 - 2018-06-07](https://www.globalkeysolutions.net/api/records/fda_inspections/mobius-medical-systems-lp/ce535aaf-c10d-4706-a71e-74a34acda9c2/)
- [FDA Inspection 984864 - 2016-08-29](https://www.globalkeysolutions.net/api/records/fda_inspections/mobius-medical-systems-lp/b14b3af0-ad94-4e18-9f0d-a0fc454cfc72/)
- [FDA Inspection 984864 - 2016-08-29](https://www.globalkeysolutions.net/api/records/fda_inspections/mobius-medical-systems-lp/7412c50c-e25e-4c1f-86dd-f51fd80fae6e/)
- [FDA Inspection 783032 - 2012-05-29](https://www.globalkeysolutions.net/api/records/fda_inspections/mobius-medical-systems-lp/7f18a8ac-c84a-40a1-9e87-c78dc814cc9f/)
- [FDA Inspection 783032 - 2012-05-29](https://www.globalkeysolutions.net/api/records/fda_inspections/mobius-medical-systems-lp/3fe54aae-998e-40e3-b654-67ddbc6dd5a2/)

Company: https://www.globalkeysolutions.net/companies/mobius-medical-systems-lp/f15e5af3-2e18-4008-ad23-56b51b759ed0

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