FDA Inspection 885429 — CDB Corporation

CDB Corporation — FEI 3003069616

The FDA completed an inspection of CDB Corporation on June 26, 2014 in Leland, NC. 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
June 26, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Leland, NC (United States)

Citations

IDCFRDescription
315921 CFR 820.184DHR content
383721 CFR 820.25(b)Training records