FDA Inspection 748649 — NIPRO CORP.

NIPRO CORP. — FEI 3002807710

The FDA completed an inspection of NIPRO CORP. on September 29, 2011 in Odate. 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
September 29, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Odate (Japan)