FDA Inspection 749173 — DiaPharma Group Inc

DiaPharma Group Inc — FEI 3000719074

The FDA completed an inspection of DiaPharma Group Inc on October 11, 2011 in West Chester, OH. 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
October 11, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
West Chester, OH (United States)