FDA Inspection 982618 — Mindways Software, Inc.

Mindways Software, Inc. — FEI 1000124212

The FDA completed an inspection of Mindways Software, Inc. on Aug 5, 2016 in Austin, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 5, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Austin, TX (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
316821 CFR 820.198(a)Complaints
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures

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