FDA Inspection 1070008 — Cytonics Corporation

Cytonics Corporation — FEI 3009327721

The FDA completed an inspection of Cytonics Corporation on Mar 21, 2018 in Jupiter, FL. 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 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jupiter, FL (United States)