FDA Inspection 984864 — Mobius Medical Systems, LP

Mobius Medical Systems, LP — FEI 3008610750

The FDA completed an inspection of Mobius Medical Systems, LP on Aug 29, 2016 in Houston, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 29, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Houston, TX (United States)

Citations

IDCFRDescription
421221 CFR 806.20(b)(4)Justification for not reporting