FDA Inspection 599707 — Clinicon Corp

Clinicon Corp — FEI 3000719724

The FDA completed an inspection of Clinicon Corp on July 14, 2009 in Oceanside, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 14, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Oceanside, CA (United States)

Citations

IDCFRDescription
330121 CFR 820.100(a)(2)Investigation procedures
53821 CFR 820.70(a)Process control procedures