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FDA Inspection 1306606 — DiaPharma Group Inc

DiaPharma Group Inc — FEI 3000719074

The FDA completed an inspection of DiaPharma Group Inc on February 25, 2026 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
February 25, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
West Chester, OH (United States)

Facility

Other inspections at this facility

  • 1171225 (VAI Fri Apr 29 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 940414 (NAI Mon Aug 31 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 749173 (NAI Tue Oct 11 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 712065 (OAI Tue Mar 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources