FDA Inspection 707223 — Cybernet Medical Corp.

Cybernet Medical Corp. — FEI 3004198411

The FDA completed an inspection of Cybernet Medical Corp. on January 10, 2011 in Ann Arbor, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 8 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 10, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ann Arbor, MI (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
315521 CFR 820.181(a)DMR device specifications
315921 CFR 820.184DHR content
316821 CFR 820.198(a)Complaints
319921 CFR 820.40(a)Document review, approval documentation
326921 CFR 820.80(b)Incoming acceptance records, documentation
333121 CFR 820.181DMR - not or inadequately maintained
383721 CFR 820.25(b)Training records