FDA Inspection 755830 — Codonics Inc

Codonics Inc — FEI 1000639866

The FDA completed an inspection of Codonics Inc on Dec 2, 2011 in Cleveland, OH. 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
Dec 2, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Cleveland, OH (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.