FDA Inspection 1083804 — CyberLogic, Inc.

CyberLogic, Inc. — FEI 3005944888

The FDA completed an inspection of CyberLogic, Inc. on March 25, 2019 in Brooklyn, NY. 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
March 25, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brooklyn, NY (United States)

Citations

IDCFRDescription
310421 CFR 820.30(j)Design history file
311721 CFR 820.70(i)Software validation for automated processes
311821 CFR 820.75(a)Documentation
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
312721 CFR 820.80(e)Documentation
320721 CFR 820.50(b)Supplier notification of changes
44721 CFR 820.40Lack of procedures, or not maintained
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures