# Mobius Medical Systems, LP – FDA Inspection, Jun 7, 2018

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

> FDA inspection 1054723 of Mobius Medical Systems, LP, June 07, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 984864 - 2016-08-29
- [FDA Inspection 783032 - 2012-05-29](https://www.keypedia.com/records/fda_inspections/mobius-medical-systems-lp/7f18a8ac-c84a-40a1-9e87-c78dc814cc9f)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

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

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