FDA Inspection 940414 — DiaPharma Group Inc

DiaPharma Group Inc — FEI 3000719074

The FDA completed an inspection of DiaPharma Group Inc on August 31, 2015 in West Chester, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 31, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
West Chester, OH (United States)

Citations

IDCFRDescription
265021 CFR 820.30(f)Design verification - Lack of or inadequate procedures