FDA Inspection
Mobius Medical Systems, LPMobius Medical Systems, LP – FDA Inspection, May 29, 2012
Record Details
This FDA Inspection record concerns Mobius Medical Systems, LP, with an inspection on May 29, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Mobius Medical Systems, LP
- Inspection Date
- May 29, 2012
- Product Type
- Devices
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ID · 7f18a8ac-c84a-40a1-9e87-c78dc814cc9f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 783032
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
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Other FDA inspections of Mobius Medical Systems, LP
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 7, 2018 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 29, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Mobius Medical Systems, LP
- FDA Inspection 1054723 - 2018-06-07
- FDA Inspection 984864 - 2016-08-29
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