FDA Inspection 849521 — Clinicon Corp

Clinicon Corp — FEI 3000719724

The FDA completed an inspection of Clinicon Corp on September 9, 2013 in Oceanside, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 9, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Oceanside, CA (United States)