FDA Inspection 870319 — Cyotcore Inc

Cyotcore Inc — FEI 3006497029

The FDA completed an inspection of Cyotcore Inc on Mar 12, 2014 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 12, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chicago, IL (United States)