# Mobius Medical Systems, LP – FDA Inspection, May 29, 2012

Source: https://www.keypedia.com/records/fda_inspections/mobius-medical-systems-lp/7f18a8ac-c84a-40a1-9e87-c78dc814cc9f
Source feed: FDA_Inspections

> FDA inspection 783032 of Mobius Medical Systems, LP, May 29, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 783032
- Company Name: Mobius Medical Systems, LP
- Inspection Date: 2012-05-29
- 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: 1

## Related Documents

- [FDA Inspection 1054723 - 2018-06-07](https://www.keypedia.com/records/fda_inspections/mobius-medical-systems-lp/f8beab0f-eb5c-4396-929f-65f695eac33c)
- FDA Inspection 984864 - 2016-08-29

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